Mayr's Database Of Reactivity Parameters
AK Prof. Mayr

Nucleophiles

Found 1302 Molecules.
Molecule Solvent Reactivity Parameters Classification Reference (sort by title or year)
image of molecule

o-nitrophenolate (in DMF)
DMFN  Parameter: 16.65
sN Parameter: 0.70
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

o-nitrophenolate (in DMSO)
DMSON  Parameter: 15.48
sN Parameter: 0.71
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-nitrophenolate (in DMF)
DMFN  Parameter: 15.05
sN Parameter: 0.80
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-nitrophenolate (in MeCN)
MeCNN  Parameter: 15.14
sN Parameter: 0.82
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

o-nitrophenolate (in MeCN)
MeCNN  Parameter: 15.83
sN Parameter: 0.80
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
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cysteine (dianionic, in water)
waterN  Parameter: 23.43
sN Parameter: 0.42
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)pinacolborate
MeCNN  Parameter: 6.24
sN Parameter: 1.00
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

potassium trifluoro(furan-2-yl)borate
MeCNN  Parameter: 5.99
sN Parameter: 0.79
**J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
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((dimethylsilyl)methyl)trimethylsilane
dichloromethaneN  Parameter: 4.86
sN Parameter: 0.64
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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((methylsilanediyl)bis(methylene))bis(trimethylsilane)
dichloromethaneN  Parameter: 4.91
sN Parameter: 0.64
**Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

(1H-inden-1-yl)trimethylsilane (in CH2Cl2)
dichloromethaneN  Parameter: -0.10
sN Parameter: 1.05
***Angew. Chem. Int. Ed. 2015, 54, 12497-12500
DOI: 10.1002/anie.201501385
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(1H-inden-1-yl)trimethylstannane (in CH2Cl2)
dichloromethaneN  Parameter: 6.68
sN Parameter: 0.81
***Angew. Chem. Int. Ed. 2015, 54, 12497-12500
DOI: 10.1002/anie.201501385
image of molecule

(1H-inden-1-yl)zinc(II) bromide*LiBr (in DMSO)
DMSON  Parameter: 15.60
sN Parameter: 0.51
**Angew. Chem. Int. Ed. 2015, 54, 12497-12500
DOI: 10.1002/anie.201501385
image of molecule

(1H-inden-1-yl)zinc(II) chloride*LiCl (in DMSO)
DMSON  Parameter: 18.10
sN Parameter: 0.46
**Angew. Chem. Int. Ed. 2015, 54, 12497-12500
DOI: 10.1002/anie.201501385
image of molecule

(1S)-(-)-alpha-pinene
dichloromethaneN  Parameter: 0.68
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(2,2-diphenylethyl)diethyl(methyl)silane
dichloromethaneN  Parameter: -6.40
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

(2,3-dimethylbut-2-enyl)triethylsilane
dichloromethaneN  Parameter: 3.15
sN Parameter: 1.15
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(2-([1,1'-biphenyl]-4-yl)ethyl)trimethylstannane
1,2-dichloroethaneN  Parameter: -0.80
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

(2-methylallyl)benzene
dichloromethaneN  Parameter: 0.25
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(2-methylallyl)dicarbonyl(cyclopentadienyl)iron(II)
dichloromethaneN  Parameter: 8.45
sN Parameter: 0.83
***Helv. Chim. Acta 2005, 88, 1754-1768
DOI: 10.1002/hlca.200590137
image of molecule

(2-methylallyl)tributylstannane
dichloromethaneN  Parameter: 7.48
sN Parameter: 0.89
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
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(2-methylallyl)trichlorosilane
dichloromethaneN  Parameter: -0.57
sN Parameter: 0.95
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(2-methylallyl)trimethylsilane
dichloromethaneN  Parameter: 4.41
sN Parameter: 0.96
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
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(2-methylallyl)triphenylgermane
dichloromethaneN  Parameter: 4.67
sN Parameter: 0.81
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
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(2-methylallyl)triphenylsilane
dichloromethaneN  Parameter: 4.17
sN Parameter: 0.79
**J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(2-methylallyl)triphenylstannane
dichloromethaneN  Parameter: 5.13
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(2-methylallyl)tris(trimethylsilyl)silane
dichloromethaneN  Parameter: 4.63
sN Parameter: 0.87
***Org. Lett. 2010, 12, 5206-5209
DOI: 10.1021/ol102220e
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(2R,5S)-5-benzyl-3-methyl-2-(5-methylfuran-2-yl)imidazolidin-4-one
MeCNN  Parameter: 7.39
sN Parameter: 1.00
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
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(2S,3S)-3-isopropyl-2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
dichloromethaneN  Parameter: 14.96
sN Parameter: 0.64
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
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(2S,5S)-5-benzyl-2-(tert-butyl)-3-methyl-1-((E)-styryl)imidazolidin-4-one
MeCNN  Parameter: 5.80
sN Parameter: 0.87
***Angew. Chem. Int. Ed. 2012, 51, 5739-5742
DOI: 10.1002/anie.201201240
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(2S,5S)-5-benzyl-2-(tert-butyl)-3-methylimidazolidin-4-one
MeCNN  Parameter: 5.44
sN Parameter: 1.12
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
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(2S,5S)-5-benzyl-3-methyl-2-(5-methylfuran-2-yl)imidazolidin-4-one
MeCNN  Parameter: 8.76
sN Parameter: 0.89
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
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(3,3,4,4,5,5,6,6,7,7,7-undecafluoro)-2-(trimethylsiloxy)hept-1-ene
dichloromethaneN  Parameter: -3.52
sN Parameter: 1.17
***Org. Lett. 2012, 14, 3990-3993
DOI: 10.1021/ol301766w
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(3-chlorobenzyl)dimethylsilane
dichloromethaneN  Parameter: 1.30
sN Parameter: 0.75
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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(4,4-dimethylpentyl)trimethylstannane
dichloromethane/MeCN mixN  Parameter: -3.90
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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(4-(tert-butyl)phenethyl)trimethylstannane
1,2-dichloroethaneN  Parameter: -0.30
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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(4-Br-C6H4)-(CO)-CH=SMe2
dichloromethaneN  Parameter: 11.95
sN Parameter: 0.76
***Angew. Chem. Int. Ed. 2009, 48, 5034-5037
DOI: 10.1002/anie.200900933
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(4-Br-C6H4)-(CO)-CH=SMe2 (in DMSO)
DMSON  Parameter: 13.78
sN Parameter: 0.72
***J. Am. Chem. Soc. 2010, 132, 17894-17900
DOI: 10.1021/ja1084749
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(4-chlorophenethyl)trimethylstannane
1,2-dichloroethaneN  Parameter: -1.80
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

(4-chlorophenyl)dimethylsilane
dichloromethaneN  Parameter: 3.05
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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(4-Me2N-C6H4)-(CO)-CH=SMe2 (in DMSO)
DMSON  Parameter: 15.68
sN Parameter: 0.65
***J. Am. Chem. Soc. 2010, 132, 17894-17900
DOI: 10.1021/ja1084749
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(4-MeO-C6H4)-(CO)-CH=SMe2 (in DMSO)
DMSON  Parameter: 14.48
sN Parameter: 0.71
***J. Am. Chem. Soc. 2010, 132, 17894-17900
DOI: 10.1021/ja1084749
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(4-methoxyphenethyl)trimethylstannane
1,2-dichloroethaneN  Parameter: 0.20
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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(4-methoxyphenyl)dimethylsilane
dichloromethaneN  Parameter: 4.23
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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(5-methyl-furan-2-yl) MDA boronate
MeCNN  Parameter: 6.38
sN Parameter: 0.86
***Chem. Sci. 2012, 3, 878-882
DOI: 10.1039/c2sc00883a
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(5-methyl-furan-2-yl) MIDA boronate
MeCNN  Parameter: 1.84
sN Parameter: 1.26
**Chem. Sci. 2012, 3, 878-882
DOI: 10.1039/c2sc00883a
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(5-methyl-furan-2-yl) pinacol boronate
MeCNN  Parameter: 2.90
sN Parameter: 0.98
***Chem. Sci. 2012, 3, 878-882
DOI: 10.1039/c2sc00883a
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(5-methyl-furan-2-yl) trifluoroborate
MeCNN  Parameter: 7.66
sN Parameter: 1.04
***Chem. Sci. 2012, 3, 878-882
DOI: 10.1039/c2sc00883a
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(5-methyl-furan-2-yl)(1,1,1-tris(methoxy)ethane)borate
MeCNN  Parameter: 12.55
sN Parameter: 0.92
***Chem. Sci. 2012, 3, 878-882
DOI: 10.1039/c2sc00883a
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(allyl)dicarbonyl(cyclopentadienyl)iron(II)
dichloromethaneN  Parameter: 6.78
sN Parameter: 0.95
***Helv. Chim. Acta 2005, 88, 1754-1768
DOI: 10.1002/hlca.200590137
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(bis(trimethylsiloxy)amino)styrene
dichloromethaneN  Parameter: 4.80
sN Parameter: 0.86
*J. Org. Chem. 2001, 66, 3196-3200
DOI: 10.1021/jo0015927
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(C6H5)-(CO)-CH=SMe2 (in DMSO)
DMSON  Parameter: 13.95
sN Parameter: 0.69
***J. Am. Chem. Soc. 2010, 132, 17894-17900
DOI: 10.1021/ja1084749
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(chloromethyl)dimethylsilane
dichloromethaneN  Parameter: 0.80
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
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(Cp*)2Zr(Me)2 - Dimethyl-bis(pentamethylcyclopentadienyl)zirconium
dichloromethaneN  Parameter: 5.49
sN Parameter: 1.06
***Chem. Eur. J. 2016, 22, 11196-11200
DOI: 10.1002/chem.201602452
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(cyclohexen-1-yl)prolinate (in MeCN)
MeCNN  Parameter: 18.86
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2010, 49, 9526-9529
DOI: 10.1002/anie.201004344
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(E)-1-(1,2-diphenylvinyl)piperidine (in MeCN)
MeCNN  Parameter: 9.94
sN Parameter: 0.86
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-1-(1,2-diphenylvinyl)pyrrolidine (in MeCN)
MeCNN  Parameter: 11.66
sN Parameter: 0.82
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-1-(2-(4-methoxyphenyl)-1-phenylvinyl)pyrrolidine (in MeCN)
MeCNN  Parameter: 11.99
sN Parameter: 0.84
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-1-(2-(4-nitrophenyl)-1-phenylvinyl)pyrrolidine (in MeCN)
MeCNN  Parameter: 10.42
sN Parameter: 0.82
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-1-(N-morpholino)propene
dichloromethaneN  Parameter: 12.06
sN Parameter: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
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(E)-1-styryl-2-(triphenylsilyl)pyrrolidine (in CH2Cl2)
dichloromethaneN  Parameter: 11.77
sN Parameter: 0.98
***J. Am. Chem. Soc. 2014, 136, 14263-14269
DOI: 10.1021/ja508065e
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(E)-1-styryl-2-tritylpyrrolidine (in CH2Cl2)
dichloromethaneN  Parameter: 10.19
sN Parameter: 1.06
***J. Am. Chem. Soc. 2014, 136, 14263-14269
DOI: 10.1021/ja508065e
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(E)-1-styrylpyrrolidine (in CH2Cl2)
dichloromethaneN  Parameter: 12.26
sN Parameter: 0.93
***J. Am. Chem. Soc. 2014, 136, 14263-14269
DOI: 10.1021/ja508065e
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(E)-1-styrylpyrrolidine (in MeCN)
MeCNN  Parameter: 13.87
sN Parameter: 0.76
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-13-(ethylthio)-6-styryl-6,12-diazadispiro[4.1.47.25]tridec-12-ene (in MeCN)
MeCNN  Parameter: 7.79
sN Parameter: 0.87
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-2,2,3,5,5-pentamethyl-1-styrylimidazolidin-4-one (in MeCN)
MeCNN  Parameter: 7.10
sN Parameter: 0.82
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-2,2,3,5,5-pentamethyl-1-styrylimidazolidine-4-thione (in MeCN)
MeCNN  Parameter: 6.49
sN Parameter: 0.83
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-2-((1-(but-1-en-1-yl)-2,2,5,5-tetramethyl-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in MeCN)
MeCNN  Parameter: 9.23
sN Parameter: 0.74
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-2-methyl-penta-1,3-diene
dichloromethaneN  Parameter: 3.09
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(E)-4-(1,2-diphenylvinyl)morpholine (in MeCN)
MeCNN  Parameter: 8.78
sN Parameter: 0.83
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-4-(2-phenyl-2-(pyrrolidin-1-yl)vinyl)benzonitrile (in MeCN)
MeCNN  Parameter: 10.63
sN Parameter: 0.84
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-4-(benzylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in CH2Cl2)
dichloromethaneN  Parameter: 7.99
sN Parameter: 0.98
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-4-(benzylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in MeCN)
MeCNN  Parameter: 8.30
sN Parameter: 0.84
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-(3-phenylbut-1-en-1-yl)-2,5-dihydro-1H-imidazole (in MeCN)
MeCNN  Parameter: 7.92
sN Parameter: 0.73
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-(3-phenylprop-1-en-1-yl)-2,5-dihydro-1H-imidazole (in MeCN)
MeCNN  Parameter: 9.64
sN Parameter: 0.70
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in CH2Cl2)
dichloromethaneN  Parameter: 8.13
sN Parameter: 0.97
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
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(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in MeCN)
MeCNN  Parameter: 8.12
sN Parameter: 0.88
***Chem. Eur. J. 2024, 30, e202302764
DOI: 10.1002/chem.202302764
image of molecule

(E)-4-styrylmorpholine
MeCNN  Parameter: 11.66
sN Parameter: 0.83
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-beta-(N-morpholino)styrene
dichloromethaneN  Parameter: 10.76
sN Parameter: 0.87
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
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(E)-beta-(N-piperidino)styrene (in MeCN)
MeCNN  Parameter: 13.84
sN Parameter: 0.73
***Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
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(E)-but-2-ene
dichloromethaneN  Parameter: -2.45
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(E)-but-2-enyltrimethylsilane
dichloromethaneN  Parameter: 1.94
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(E)-penta-1,3-diene
dichloromethaneN  Parameter: 1.49
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(E)-propenylbenzene
dichloromethaneN  Parameter: -0.49
sN Parameter: 1.18
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
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(E,E)-2,5-heptadiene
dichloromethaneN  Parameter: -0.74
sN Parameter: 0.99
***J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
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(E,E)-hexa-2,4-diene
dichloromethaneN  Parameter: 1.17
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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(EtO)2P(O)CH(-)CN (in DMSO)
DMSON  Parameter: 18.57
sN Parameter: 0.66
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
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(EtO)2P(O)CH(-)CO2Et (in DMSO)
DMSON  Parameter: 19.23
sN Parameter: 0.65
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
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(p-bromophenyl)diazomethane
dichloromethaneN  Parameter: 8.87
sN Parameter: 0.82
***J. Am. Chem. Soc. 2018, 140, 16758-16772
DOI: 10.1021/jacs.8b09995
image of molecule

(p-cyanophenyl)diazomethane
dichloromethaneN  Parameter: 7.66
sN Parameter: 0.80
***J. Am. Chem. Soc. 2018, 140, 16758-16772
DOI: 10.1021/jacs.8b09995
image of molecule

(p-nitrophenyl)diazomethane
dichloromethaneN  Parameter: 7.17
sN Parameter: 0.83
***J. Am. Chem. Soc. 2018, 140, 16758-16772
DOI: 10.1021/jacs.8b09995
image of molecule

(R)-2-(tert-butyl)-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
dichloromethaneN  Parameter: 12.95
sN Parameter: 0.58
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

(R)-2-benzhydryl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
dichloromethaneN  Parameter: 15.30
sN Parameter: 0.55
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

(R)-2-isopropyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
dichloromethaneN  Parameter: 16.50
sN Parameter: 0.48
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

(R)-2-isopropylpyrrolidine
MeCNN  Parameter: 16.44
sN Parameter: 0.71
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-1-(3,5-bis(trifluoromethyl)phenyl)-3-(pyrrolidin-2-ylmethyl)thiourea
MeCNN  Parameter: 14.97
sN Parameter: 0.69
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
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(S)-1-(3,5-bis(trifluoromethyl)phenyl)-3-(pyrrolidin-2-ylmethyl)urea
MeCNN  Parameter: 17.50
sN Parameter: 0.64
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-1-(pyrrolidin-2-ylmethyl)-1H-imidazole
MeCNN  Parameter: 15.55
sN Parameter: 0.69
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-1-(pyrrolidin-2-ylmethyl)pyrrolidine
MeCNN  Parameter: 18.33
sN Parameter: 0.64
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-2-(azidodiphenylmethyl)pyrrolidine
MeCNN  Parameter: 9.90
sN Parameter: 1.22
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-2-(azidomethyl)pyrrolidine
MeCNN  Parameter: 15.43
sN Parameter: 0.73
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-2-(diphenyl((trimethylsilyl)oxy)methyl)pyrrolidine
MeCNN  Parameter: 12.03
sN Parameter: 0.98
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-2-(methoxymethyl)pyrrolidine
MeCNN  Parameter: 16.50
sN Parameter: 0.71
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-2-(pyrrolidin-2-ylmethyl)isoindoline-1,3-dione
MeCNN  Parameter: 15.90
sN Parameter: 0.77
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-2-benzhydrylpyrrolidine
MeCNN  Parameter: 16.61
sN Parameter: 0.67
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
dichloromethaneN  Parameter: 13.45
sN Parameter: 0.72
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

(S)-3,3-difluoro-2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine (in CH2Cl2)
dichloromethaneN  Parameter: 10.83
sN Parameter: 0.80
***ARKIVOC 2024, (4), 202312093
DOI: 10.24820/ark.5550190.p012.093
image of molecule

(S)-3-butyl-1-(pyrrolidin-2-ylmethyl)-1H-imidazol-3-ium trifluoromethanesulfonate
MeCNN  Parameter: 13.57
sN Parameter: 0.53
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-4-benzyl-1,3-oxazolidin-2-one anion (in DMSO)
DMSON  Parameter: 22.67
sN Parameter: 0.54
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

(S)-4-phenyl-1-(pyrrolidin-2-ylmethyl)-1H-1,2,3-triazole
MeCNN  Parameter: 15.32
sN Parameter: 0.72
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one
MeCNN  Parameter: 6.04
sN Parameter: 0.92
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-diphenyl(pyrrolidin-2-yl)methanol
MeCNN  Parameter: 16.18
sN Parameter: 0.56
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-N,N-dimethyl-1-(pyrrolidin-2-yl)methanamine
MeCNN  Parameter: 17.41
sN Parameter: 0.68
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-N,N-dimethylpyrrolidine-2-carboxamide
MeCNN  Parameter: 17.61
sN Parameter: 0.67
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-N-propylpyrrolidine-2-carboxamide
MeCNN  Parameter: 15.20
sN Parameter: 0.73
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-pyrrolidin-2-ylmethanamine
MeCNN  Parameter: 17.24
sN Parameter: 0.67
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S)-pyrrolidin-2-ylmethanol
MeCNN  Parameter: 16.74
sN Parameter: 0.67
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

(S,E)-2-(diphenyl(trimethylsiloxy)methyl)-1-styrylpyrrolidine
MeCNN  Parameter: 10.56
sN Parameter: 1.01
***Angew. Chem. Int. Ed. 2012, 51, 5739-5742
DOI: 10.1002/anie.201201240
image of molecule

(S,E)-3-benzyl-1-methyl-4-styryl-1,4-diazaspiro[4.4]nonan-2-one
MeCNN  Parameter: 7.92
sN Parameter: 1.07
***Angew. Chem. Int. Ed. 2012, 51, 5739-5742
DOI: 10.1002/anie.201201240
image of molecule

(S,E)-5-benzyl-2,2,3-trimethyl-1-styrylimidazolidin-4-one
MeCNN  Parameter: 7.20
sN Parameter: 1.14
***Angew. Chem. Int. Ed. 2012, 51, 5739-5742
DOI: 10.1002/anie.201201240
image of molecule

(triisopropylsiloxy)ethene
dichloromethaneN  Parameter: 3.44
sN Parameter: 0.94
**J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(trimethylsilyl)diazomethane
dichloromethaneN  Parameter: 8.97
sN Parameter: 0.75
***Chem. Eur. J. 2003, 9, 4068-4076
DOI: 10.1002/chem.200304913
image of molecule

(tris(trimethylsilyl)siloxy)ethene
dichloromethaneN  Parameter: 4.01
sN Parameter: 0.83
***Org. Lett. 2010, 12, 5206-5209
DOI: 10.1021/ol102220e
image of molecule

(Z)-1,2-diphenyl-1-(trimethylsiloxy)ethene (in MeCN)
MeCNN  Parameter: 3.00
sN Parameter: 0.83
***Synthesis 2019, 51, 1157-1170
DOI: 10.1055/s-0037-1611634
image of molecule

(Z)-1-(1,3-dimesityl-1H-imidazol-3-ium-2-yl)-2-phenylprop-1-en-1-olate (in DMSO)
DMSON  Parameter: 14.40
sN Parameter: 0.64
***Angew. Chem. Int. Ed. 2013, 52, 11163-11167
DOI: 10.1002/ange.201303524
image of molecule

(Z)-1-(1,3-dimesityl-1H-imidazol-3-ium-2-yl)-2-phenylprop-1-en-1-olate (in THF)
THFN  Parameter: 15.33
sN Parameter: 0.79
***Angew. Chem. Int. Ed. 2013, 52, 11163-11167
DOI: 10.1002/ange.201303524
image of molecule

(Z)-1-(1,3-dimesityl-4,5-dihydro-1H-imidazol-3-ium-2-yl)-2-phenylprop-1-en-1-olate (in THF)
THFN  Parameter: 15.92
sN Parameter: 0.72
***Angew. Chem. Int. Ed. 2013, 52, 11163-11167
DOI: 10.1002/ange.201303524
image of molecule

(Z)-1-(N-morpholino)propene
dichloromethaneN  Parameter: 12.26
sN Parameter: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

(Z)-1-(triisopropylsiloxy)propen
dichloromethaneN  Parameter: 3.87
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

(Z)-1-phenyl-1-(trimethylsiloxy)propene (in MeCN)
MeCNN  Parameter: 5.18
sN Parameter: 0.94
***Synthesis 2019, 51, 1157-1170
DOI: 10.1055/s-0037-1611634
image of molecule

(Z)-2-phenyl-1-(1,3,4-triphenyl-4H-1,2,4-triazol-1-ium-5-yl)prop-1-en-1-olate (in THF)
THFN  Parameter: 14.40
sN Parameter: 0.66
***Angew. Chem. Int. Ed. 2013, 52, 11163-11167
DOI: 10.1002/ange.201303524
image of molecule

(Z)-2-phenyl-1-(1,3,4-triphenyl-4H-1,2,4-triazol-1-ium-5-yl)prop-1-en-1-olate (in THF)
THFN  Parameter: 16.73
sN Parameter: 0.63
**Angew. Chem. Int. Ed. 2013, 52, 11163-11167
DOI: 10.1002/ange.201303524
image of molecule

(Z)-but-2-ene
dichloromethaneN  Parameter: -2.44
sN Parameter: 1.09
**J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(Z)-but-2-enyltrimethylsilane
dichloromethaneN  Parameter: 1.69
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

(Z)-penta-1,3-diene
dichloromethaneN  Parameter: 0.66
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

(Z)-phenylpropene
dichloromethaneN  Parameter: -1.07
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

1% water/99% HFIP (w/w)
water-HFIP mixN  Parameter: -1.93
sN Parameter: 1.09
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

1,1,1,3,3,3-hexamethyl-2-(trimethylsilyl)trisilane
dichloromethaneN  Parameter: 3.61
sN Parameter: 0.79
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,1,1,3,3-pentamethyldisiloxane
dichloromethaneN  Parameter: 3.12
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,1,3,3-tetramethylguanidine
dichloromethaneN  Parameter: 13.58
sN Parameter: 0.77
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

1,1-bis(trimethylsiloxy)propene
dichloromethaneN  Parameter: 10.38
sN Parameter: 0.87
****Eur. J. Org. Chem. 2004, , 2791-2796
DOI: 10.1002/ejoc.200400134
image of molecule

1,1-diethoxyethene
dichloromethaneN  Parameter: 9.81
sN Parameter: 0.81
***Eur. J. Org. Chem. 2004, , 2791-2796
DOI: 10.1002/ejoc.200400134
image of molecule

1,1-dimethyl-2-methylenehydrazine (in CH2Cl2)
dichloromethaneN  Parameter: 6.98
sN Parameter: 0.85
***Angew. Chem. Int. Ed. 2013, 52, 11900-11904
DOI: 10.1002/anie.201305092
image of molecule

1,1-dimethyl-2-methylenehydrazine (in CH2Cl2)
dichloromethaneN  Parameter: 19.31
sN Parameter: 0.46
***Angew. Chem. Int. Ed. 2013, 52, 11900-11904
DOI: 10.1002/anie.201305092
image of molecule

1,1-dimethylhydrazine (in MeCN)
MeCNN  Parameter: 11.72
sN Parameter: 0.73
***Angew. Chem. Int. Ed. 2012, 51, 1353-1356
DOI: 10.1002/anie.201107315
image of molecule

1,1-dimethylhydrazine (in MeCN)
MeCNN  Parameter: 22.41
sN Parameter: 0.45
***Angew. Chem. Int. Ed. 2012, 51, 1353-1356
DOI: 10.1002/anie.201107315
image of molecule

1,1-dimethylsilepane
dichloromethaneN  Parameter: -3.10
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,1-dimethylsiletane
dichloromethaneN  Parameter: -2.10
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,1-dimethylsilinane
dichloromethaneN  Parameter: -2.40
sN Parameter: 1.10
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,1-dimethylsilolane
dichloromethaneN  Parameter: -3.86
sN Parameter: 1.10
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyrimidine (TBN)
dichloromethaneN  Parameter: 16.15
sN Parameter: 0.73
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

1,2,3-trimethoxy-1,3-dioxopropan-2-ide (in DMSO)
DMSON  Parameter: 20.08
sN Parameter: 0.74
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

1,2,4,5-tetramethylcyclohexa-1,4-diene (in CH2Cl2)
dichloromethaneN  Parameter: 4.27
sN Parameter: 0.86
**J. Am. Chem. Soc. 2014, 136, 13863-13873
DOI: 10.1021/ja507598y
image of molecule

1,2,5-trimethylpyrrole
MeCNN  Parameter: 8.69
sN Parameter: 1.07
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092
image of molecule

1,2-bis(trimethylsiloxy)cyclohexene
dichloromethaneN  Parameter: 4.46
sN Parameter: 1.15
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

1,2-dihydronaphthalene (in MeCN)
MeCNN  Parameter: -3.30
sN Parameter: 1.00
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,2-dimethylhydrazine (in MeCN)
MeCNN  Parameter: 16.15
sN Parameter: 0.68
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

1,2-dimethylindole
dichloromethaneN  Parameter: 6.54
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

1,3,4-triphenyl-1H-1,2,4-triazol-4-ium-5-ide (in THF)
THFN  Parameter: 14.07
sN Parameter: 0.84
***Angew. Chem. Int. Ed. 2011, 50, 6915-6919
DOI: 10.1002/anie.201102435
image of molecule

1,3,5-trimethyl-2-methylene-1,2-dihydropyridine (in DMSO)
DMSON  Parameter: 21.16
sN Parameter: 0.59
***Eur. J. Org. Chem. 2024, 27, e202400373
DOI: 10.1002/ejoc.202400373
image of molecule

1,3,5-trimethylcyclohexa-1,4-diene (in CH2Cl2)
dichloromethaneN  Parameter: 4.95
sN Parameter: 0.79
**J. Am. Chem. Soc. 2014, 136, 13863-13873
DOI: 10.1021/ja507598y
image of molecule

1,3-bis(2,6-diisopropylphenyl)-2,3-dihydro-1H-1,3,2-diazaphosphole (in MeCN)
MeCNN  Parameter: 19.85
sN Parameter: 0.34
***Angew. Chem. Int. Ed. 2019, 58, 5983-5987
DOI: 10.1002/anie.201901456
image of molecule

1,3-Bis(2,6-diisopropylphenyl)-4-methylene-5-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)
THFN  Parameter: 22.30
sN Parameter: 0.49
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

1,3-bis(2,6-diisopropylphenyl)-4-methylene-5-phenyl-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)
THFN  Parameter: 22.80
sN Parameter: 0.60
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

1,3-Bis(2,6-diisopropylphenyl)-5-(4-methoxyphenyl)-4-methylene-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)
THFN  Parameter: 23.55
sN Parameter: 0.56
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

1,3-bis(2,6-diisopropylphenyl)-5-methyl-4-methylene-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)
THFN  Parameter: 24.86
sN Parameter: 0.52
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

1,3-Bis(2,6-diisopropylphenyl)-5-methylene-4-(2,4,6-triisopropylphenyl)-4,5-dihydro-1H-1,2,3-triazol-3-ium-4-ide (in THF)
THFN  Parameter: 21.36
sN Parameter: 0.42
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

1,3-Bis(2,6-diisopropylphenyl)-5-methylene-4-(2,4,6-triisopropylphenyl)-4,5-dihydro-1H-1,2,3-triazol-3-ium-4-ide (in THF)
THFN  Parameter: 20.78
sN Parameter: 0.61
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

1,3-bis(trimethylgermyl)propane (in MeCN)
MeCNN  Parameter: -3.40
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,3-bis(trimethylsilyl)propane
dichloromethane/MeCN mixN  Parameter: -5.30
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,3-bis(trimethylstannyl)propane (in MeCN)
MeCNN  Parameter: -1.70
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,3-di-tert-butyl-1,3,2-diazaphosphinane (in MeCN)
MeCNN  Parameter: 13.46
sN Parameter: 0.52
***Angew. Chem. Int. Ed. 2019, 58, 5983-5987
DOI: 10.1002/anie.201901456
image of molecule

1,3-di-tert-butyl-1,3,2-diazaphospholidine (in MeCN)
MeCNN  Parameter: 18.74
sN Parameter: 0.47
***Angew. Chem. Int. Ed. 2019, 58, 5983-5987
DOI: 10.1002/anie.201901456
image of molecule

1,3-di-tert-butyl-2,3-dihydro-1H-1,3,2-diazaphosphole (in MeCN)
MeCNN  Parameter: 25.54
sN Parameter: 0.35
***Angew. Chem. Int. Ed. 2019, 58, 5983-5987
DOI: 10.1002/anie.201901456
image of molecule

1,3-di-tert-butyl-2,3-dihydro-1H-benzo[d][1,3,2]diazaphosphole (in MeCN)
MeCNN  Parameter: 20.93
sN Parameter: 0.43
***Angew. Chem. Int. Ed. 2019, 58, 5983-5987
DOI: 10.1002/anie.201901456
image of molecule

1,3-diaminopropane (in water)
waterN  Parameter: 14.02
sN Parameter: 0.54
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

1,3-diethoxy-2-fluoro-1,3-dioxopropan-2-ide (in DMSO)
DMSON  Parameter: 20.63
sN Parameter: 0.76
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

1,3-diethyl-thiobarbiturate anion (in DMSO)
DMSON  Parameter: 14.90
sN Parameter: 0.80
***J. Org. Chem. 2017, 82, 8476-8488
DOI: 10.1021/acs.joc.7b01223
image of molecule

1,3-Diisopropyl-4-methylene-5-phenyl-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)
THFN  Parameter: 30.25
sN Parameter: 0.54
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

1,3-dimesityl-1H-imidazol-3-ium-2-ide (in THF)
THFN  Parameter: 21.72
sN Parameter: 0.45
***Angew. Chem. Int. Ed. 2011, 50, 6915-6919
DOI: 10.1002/anie.201102435
image of molecule

1,3-dimesityl-2,3-dihydro-1H-1,3,2-diazaphosphole (in MeCN)
MeCNN  Parameter: 17.68
sN Parameter: 0.68
***Angew. Chem. Int. Ed. 2019, 58, 5983-5987
DOI: 10.1002/anie.201901456
image of molecule

1,3-dimesityl-2-methylene-2,3-dihydro-1H-imidazole (in THF)
THFN  Parameter: 17.80
sN Parameter: 0.79
***J. Org. Chem. 2021, 86, 2974-2985
DOI: 10.1021/acs.joc.0c02838
image of molecule

1,3-dimesityl-4,5-dihydro-1H-imidazol-3-ium-2-ide (in THF)
THFN  Parameter: 23.35
sN Parameter: 0.40
***Angew. Chem. Int. Ed. 2011, 50, 6915-6919
DOI: 10.1002/anie.201102435
image of molecule

1,3-dimethoxybenzene
dichloromethaneN  Parameter: 2.48
sN Parameter: 1.09
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1,3-dimethyl-2-methylene-1,2-dihydropyridine (in DMSO)
DMSON  Parameter: 19.91
sN Parameter: 0.62
***Eur. J. Org. Chem. 2024, 27, e202400373
DOI: 10.1002/ejoc.202400373
image of molecule

1,3-dimethyl-2-methylene-1,2-dihydropyridine (in MeCN)
MeCNN  Parameter: 19.69
sN Parameter: 0.61
***Eur. J. Org. Chem. 2024, 27, e202400373
DOI: 10.1002/ejoc.202400373
image of molecule

1,3-dimethyl-2-methylene-2,3-dihydro-1H-benzo[d]imidazole
THFN  Parameter: 19.84
sN Parameter: 0.58
***J. Org. Chem. 2021, 86, 2974-2985
DOI: 10.1021/acs.joc.0c02838
image of molecule

1,3-dimethyl-2-methylenehexahydropyrimidine (in THF)
THFN  Parameter: 18.68
sN Parameter: 0.63
***J. Org. Chem. 2021, 86, 2974-2985
DOI: 10.1021/acs.joc.0c02838
image of molecule

1,3-dimethyl-2-methyleneimidazolidine (in THF)
THFN  Parameter: 18.11
sN Parameter: 0.68
***J. Org. Chem. 2021, 86, 2974-2985
DOI: 10.1021/acs.joc.0c02838
image of molecule

1,3-dimethylbarbiturate anion (in DMSO)
DMSON  Parameter: 17.46
sN Parameter: 0.72
***J. Org. Chem. 2017, 82, 8476-8488
DOI: 10.1021/acs.joc.7b01223
image of molecule

1,3-dimethylimidazolidin-2-imine
dichloromethaneN  Parameter: 12.46
sN Parameter: 0.87
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

1,3-dioxepane
dichloromethaneN  Parameter: -3.80
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,3-dioxolane
dichloromethaneN  Parameter: -2.86
sN Parameter: 0.80
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,3-oxazolidin-2-one anion (in DMSO)
DMSON  Parameter: 22.40
sN Parameter: 0.59
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

1,4-cyclohexadiene
dichloromethaneN  Parameter: 0.09
sN Parameter: 0.98
***J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

1,4-cyclohexadiene (in MeCN)
MeCNN  Parameter: 0.35
sN Parameter: 0.98
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,4-dihydronaphthalene
dichloromethaneN  Parameter: -0.07
sN Parameter: 1.03
***J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

1,4-dihydronaphthalene (in MeCN)
MeCNN  Parameter: -2.50
sN Parameter: 1.00
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,4-dimethylcyclohexa-1,4-diene (in CH2Cl2)
dichloromethaneN  Parameter: 1.88
sN Parameter: 0.96
**J. Am. Chem. Soc. 2014, 136, 13863-13873
DOI: 10.1021/ja507598y
image of molecule

1,4-pentadiene
dichloromethaneN  Parameter: -2.99
sN Parameter: 0.97
*J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

1,6-bis(trimethylsilyl)hexane
dichloromethaneN  Parameter: -4.70
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1,6-dimethyl-2-methylene-1,2-dihydropyridine (in DMSO)
DMSON  Parameter: 20.76
sN Parameter: 0.60
***Eur. J. Org. Chem. 2024, 27, e202400373
DOI: 10.1002/ejoc.202400373
image of molecule

1-((4-chlorobenzylidene)amino)-2-ethoxy-2-oxoethan-1-ide (in DMSO)
DMSON  Parameter: 29.02
sN Parameter: 0.49
**Tetrahedron 2019, 75, 459-463
DOI: 10.1016/j.tet.2018.11.075
image of molecule

1-((diphenylmethylene)amino)-2-ethoxy-2-oxoethan-1-ide (in DMSO)
DMSON  Parameter: 26.95
sN Parameter: 0.52
***Tetrahedron 2019, 75, 459-463
DOI: 10.1016/j.tet.2018.11.075
image of molecule

1-(1-cyclohexenyl)-4-methylpiperazine
dichloromethaneN  Parameter: 12.51
sN Parameter: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-(2-methyl-4,5-dihydro-1H-imidazol-1-yl)ethanone (in CH2Cl2)
dichloromethaneN  Parameter: 10.03
sN Parameter: 0.75
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

1-(3-chloropyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-ide (in DMSO)
DMSON  Parameter: 17.98
sN Parameter: 0.63
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

1-(4-(dimethylamino)pyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-ide (in DMSO)
DMSON  Parameter: 21.61
sN Parameter: 0.58
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

1-(4-(tert-butyl)phenyl)-2-methylene-4,6-diphenyl-1,2-dihydropyridine (in DMSO)
DMSON  Parameter: 19.36
sN Parameter: 0.68
***Eur. J. Org. Chem. 2024, 27, e202400373
DOI: 10.1002/ejoc.202400373
image of molecule

1-(benzylideneamino)-2-ethoxy-2-oxoethan-1-ide (in DMSO)
DMSON  Parameter: 29.10
sN Parameter: 0.50
*Tetrahedron 2019, 75, 459-463
DOI: 10.1016/j.tet.2018.11.075
image of molecule

1-(ethoxycarbonyl)-2-oxocyclododecan-1-ide (in DMSO)
DMSON  Parameter: 20.60
sN Parameter: 0.63
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

1-(ethoxycarbonyl)-2-oxocycloheptan-1-ide
DMSON  Parameter: 19.53
sN Parameter: 0.83
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

1-(ethoxycarbonyl)-2-oxocyclohexan-1-ide (in DMSO)
DMSON  Parameter: 18.32
sN Parameter: 0.84
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

1-(ethoxycarbonyl)-2-oxocyclooctan-1-ide (in DMSO)
DMSON  Parameter: 20.02
sN Parameter: 0.76
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

1-(ethoxycarbonyl)-2-oxocyclopentan-1-ide (in DMSO)
DMSON  Parameter: 18.63
sN Parameter: 0.82
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

1-(isoquinolin-2-ium-2-yl)-2-oxo-2-phenylethan-1-ide (in DMSO)
DMSON  Parameter: 20.08
sN Parameter: 0.57
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

1-(N-morpholino)cyclohexene
dichloromethaneN  Parameter: 11.40
sN Parameter: 0.83
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-(N-morpholino)cyclopentene
dichloromethaneN  Parameter: 13.41
sN Parameter: 0.82
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-(N-piperidino)cyclohexene
dichloromethaneN  Parameter: 13.36
sN Parameter: 0.81
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-(N-piperidino)cyclohexene (in MeCN)
MeCNN  Parameter: 14.02
sN Parameter: 0.76
***J. Am. Chem. Soc. 2013, 135, 6579-6587
DOI: 10.1021/ja401106x
image of molecule

1-(N-piperidino)cyclopentene
dichloromethaneN  Parameter: 15.06
sN Parameter: 0.82
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-(N-pyrrolidino)cyclohexene
dichloromethaneN  Parameter: 14.91
sN Parameter: 0.86
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-(N-pyrrolidino)cyclohexene (in MeCN)
MeCNN  Parameter: 16.42
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2010, 49, 9526-9529
DOI: 10.1002/anie.201004344
image of molecule

1-(N-pyrrolidino)cyclopentene
dichloromethaneN  Parameter: 15.91
sN Parameter: 0.86
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-(p-tolyl)-1-(trimethylsilyl)ethene
dichloromethaneN  Parameter: -0.65
sN Parameter: 1.59
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

1-(perfluorophenyl)-1-(trimethylsiloxy)ethene
dichloromethaneN  Parameter: 1.47
sN Parameter: 0.89
***Org. Lett. 2012, 14, 3990-3993
DOI: 10.1021/ol301766w
image of molecule

1-(phenylethynyl)pyrrolidin-2-one
dichloromethaneN  Parameter: 3.12
sN Parameter: 0.85
*Angew. Chem. Int. Ed. 2014, 53, 4968-4971
DOI: 10.1002/anie.201402055
image of molecule

1-(phenylmethylamino)cyclohexene
dichloromethaneN  Parameter: 10.73
sN Parameter: 0.81
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-(phenylmethylamino)cyclopentene
dichloromethaneN  Parameter: 12.90
sN Parameter: 0.79
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-(trimethylsiloxy)-3,4-dihydronaphthalene (in MeCN)
MeCNN  Parameter: 5.06
sN Parameter: 0.91
***Synthesis 2019, 51, 1157-1170
DOI: 10.1055/s-0037-1611634
image of molecule

1-(trimethylsiloxy)buta-1,3-diene
dichloromethaneN  Parameter: 4.60
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

1-(trimethylsiloxy)cycloheptene
dichloromethaneN  Parameter: 6.62
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

1-(trimethylsiloxy)cyclohexene
dichloromethaneN  Parameter: 5.21
sN Parameter: 1.00
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-(trimethylsiloxy)cyclooctene
dichloromethaneN  Parameter: 6.77
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

1-(trimethylsiloxy)cyclopentene
dichloromethaneN  Parameter: 6.57
sN Parameter: 0.93
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-(trimethylsiloxy)cyclopentene (in MeCN)
MeCNN  Parameter: 6.43
sN Parameter: 0.89
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
image of molecule

1-(trimethylsilyl)-imidazole (in MeCN)
MeCNN  Parameter: 11.43
sN Parameter: 0.79
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

1-(triphenylsiloxy)cyclopentene
dichloromethaneN  Parameter: 5.76
sN Parameter: 1.02
****Eur. J. Org. Chem. 2005, , 1760-1764
DOI: 10.1002/ejoc.200400706
image of molecule

1-(tris(pentafluorophenyl)siloxy)-cyclopentene
dichloromethaneN  Parameter: 1.38
sN Parameter: 0.93
*Eur. J. Org. Chem. 2005, , 1760-1764
DOI: 10.1002/ejoc.200400706
image of molecule

1-(tris(trimethylsilyl)siloxy)cyclohexene
dichloromethaneN  Parameter: 5.07
sN Parameter: 0.91
***Org. Lett. 2010, 12, 5206-5209
DOI: 10.1021/ol102220e
image of molecule

1-aminopropan-2-ol (in DMSO)
DMSON  Parameter: 15.47
sN Parameter: 0.65
***J. Am. Chem. Soc. 2009, 131, 11392-11401
DOI: 10.1021/ja903207b
image of molecule

1-benzyl-2-phenyl-4,5-dihydro-1H-imidazole (in CH2Cl2)
dichloromethaneN  Parameter: 13.11
sN Parameter: 0.83
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

1-butoxy-1-(t-butyl-dimethylsiloxy)ethene
dichloromethaneN  Parameter: 10.32
sN Parameter: 0.79
****Eur. J. Org. Chem. 2004, , 2791-2796
DOI: 10.1002/ejoc.200400134
image of molecule

1-butoxy-1-(trimethylsiloxy)ethene
dichloromethaneN  Parameter: 10.21
sN Parameter: 0.82
****Eur. J. Org. Chem. 2004, , 2791-2796
DOI: 10.1002/ejoc.200400134
image of molecule

1-ethinylcyclohexenyl-Co2(CO)6
dichloromethaneN  Parameter: -0.44
sN Parameter: 1.06
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-ethoxy-2-methyl-1,3-dioxobutan-2-ide (in DMSO)
DMSON  Parameter: 19.58
sN Parameter: 0.73
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

1-ethoxy-3-(4-nitrophenyl)-1,3-dioxopropan-2-ide (in DMSO)
DMSON  Parameter: 16.26
sN Parameter: 0.83
***J. Am. Chem. Soc. 2018, 140, 11474-11486
DOI: 10.1021/jacs.8b07147
image of molecule

1-hexene
dichloromethaneN  Parameter: -2.77
sN Parameter: 1.41
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

1-mesityl-3-methyl-5-methylene-2,4,6-triphenyl-2,5-dihydropyridin-1-ium-2-ide (in THF)
THFN  Parameter: 26.16
sN Parameter: 0.52
***Angew. Chem. Int. Ed. 2024, , e202318283
DOI: 10.1002/anie.202318283
image of molecule

1-methoxy-2-methyl-1-(trimethylsiloxy)propene
dichloromethaneN  Parameter: 9.00
sN Parameter: 0.98
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-methoxy-2-methyl-1-(trimethylsiloxy)propene (in MeCN)
MeCNN  Parameter: 9.11
sN Parameter: 0.88
***J. Am. Chem. Soc. 2013, 135, 6579-6587
DOI: 10.1021/ja401106x
image of molecule

1-methyl uracil anion (in DMSO)
DMSON  Parameter: 16.36
sN Parameter: 0.69
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

1-methyl uracil anion (in water)
waterN  Parameter: 8.54
sN Parameter: 0.77
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

1-methyl-2,3,4,6,7,8-hexahydro-1H-pyrimido[1,2-a]pyrimidine (MeTBD)
dichloromethaneN  Parameter: 14.43
sN Parameter: 0.81
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

1-methyl-2-methylene-3-phenyl-1,2-dihydropyridine (in DMSO)
DMSON  Parameter: 19.41
sN Parameter: 0.61
***Eur. J. Org. Chem. 2024, 27, e202400373
DOI: 10.1002/ejoc.202400373
image of molecule

1-methyl-2-phenylpyrrolidine (in CH2Cl2)
dichloromethaneN  Parameter: 16.80
sN Parameter: 0.49
***J. Phys. Org. Chem. 2016, 29, 759-767
DOI: 10.1002/poc.3580
image of molecule

1-methyl-2-phenylpyrrolidine (in MeCN)
MeCNN  Parameter: 15.70
sN Parameter: 0.54
***J. Phys. Org. Chem. 2016, 29, 759-767
DOI: 10.1002/poc.3580
image of molecule

1-methyl-4-(N-morpholino)tetrahydropyridine
dichloromethaneN  Parameter: 12.03
sN Parameter: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

1-methyl-4-vinyl-benzene
dichloromethaneN  Parameter: 1.70
sN Parameter: 1.06
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-methyl-benzimidazole (in MeCN)
MeCNN  Parameter: 10.37
sN Parameter: 0.82
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

1-methyl-benzotriazole (in MeCN)
MeCNN  Parameter: 7.77
sN Parameter: 0.76
*Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

1-methyl-imidazole (in MeCN)
MeCNN  Parameter: 11.90
sN Parameter: 0.73
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

1-methyl-imidazole (in water)
waterN  Parameter: 9.91
sN Parameter: 0.55
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

1-methylcyclohexene
dichloromethaneN  Parameter: 0.08
sN Parameter: 1.15
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-methylcyclopentene
dichloromethaneN  Parameter: 1.18
sN Parameter: 1.17
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

1-methylsiletane
dichloromethaneN  Parameter: 2.30
sN Parameter: 0.75
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1-methylsilolane
dichloromethaneN  Parameter: 2.20
sN Parameter: 0.75
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1-phenoxy-1-(trimethylsiloxy)ethene
dichloromethaneN  Parameter: 8.23
sN Parameter: 0.81
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-phenyl-1-(trimethylsiloxy)ethene
dichloromethaneN  Parameter: 6.22
sN Parameter: 0.96
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

1-phenyl-imidazole (in MeCN)
MeCNN  Parameter: 11.31
sN Parameter: 0.67
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

1-phenyl-N-(phenylmethyl)methanimine (in CH2Cl2)
dichloromethaneN  Parameter: 7.90
sN Parameter: 0.76
**Z. Naturforsch. B 2013, 68b, 693-699
DOI: 10.5560/ZNB.2013-3085
image of molecule

1-pyrrolidino-3,4-dihydronaphthalene (in MeCN)
MeCNN  Parameter: 14.09
sN Parameter: 0.66
***Synthesis 2019, 51, 1157-1170
DOI: 10.1055/s-0037-1611634
image of molecule

10% ethanol/90% MeCN (v/v)
EtOH-MeCN mixN  Parameter: 5.19
sN Parameter: 0.96
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

10% methanol/90% MeCN (v/v)
MeOH-MeCN mixN  Parameter: 5.55
sN Parameter: 0.97
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

10% water/90% acetone (v/v)
water-acetone mixN  Parameter: 5.70
sN Parameter: 0.85
***Angew. Chem. Int. Ed. 2004, 43, 2302-2305
DOI: 10.1002/anie.200353468
image of molecule

10% water/90% HFIP (w/w)
water-HFIP mixN  Parameter: 0.96
sN Parameter: 0.93
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

10% water/90% MeCN (v/v)
water-MeCN mixN  Parameter: 4.56
sN Parameter: 0.94
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

10% water/90%EtOH (v/v)
water-EtOH mixN  Parameter: 7.03
sN Parameter: 0.86
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

10% water/90%TFE (v/v)
water-TFE mixN  Parameter: 2.93
sN Parameter: 0.88
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

10-methyl-9,10-dihydroacridine
dichloromethaneN  Parameter: 5.54
sN Parameter: 0.90
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

10-methyl-9,10-dihydroacridine (in MeCN)
MeCNN  Parameter: 4.00
sN Parameter: 0.70
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

1H-indole-5-carboxylic acid
MeCNN  Parameter: 3.97
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

2% water/98% HFIP (w/w)
water-HFIP mixN  Parameter: -1.62
sN Parameter: 1.10
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

2,2,2-trifluoroethanolate (in water)
waterN  Parameter: 12.66
sN Parameter: 0.59
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

2,2,2-trifluoroethylamine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 10.20
sN Parameter: 0.92
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

2,2,2-trifluoroethylamine (in DMSO)
DMSON  Parameter: 12.15
sN Parameter: 0.65
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

2,2,2-trifluoroethylamine (in MeCN)
MeCNN  Parameter: 10.13
sN Parameter: 0.75
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

2,2-dimethyl-5-(4-nitrobenzyl)-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)
DMSON  Parameter: 12.02
sN Parameter: 1.17
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

2,2-dimethylpyrrolidine
MeCNN  Parameter: 13.96
sN Parameter: 0.76
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

2,3,3-trimethyl-but-1-ene
dichloromethaneN  Parameter: 0.06
sN Parameter: 1.07
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2,3,4,6,7,8-hexahydro-1H-pyrimido[1,2-a]pyrimidine
dichloromethaneN  Parameter: 16.16
sN Parameter: 0.75
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

2,3,4,6,7,8-hexahydropyrimido[2,1-b][1,3]thiazine
dichloromethaneN  Parameter: 14.10
sN Parameter: 0.82
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole (TBO)
dichloromethaneN  Parameter: 14.44
sN Parameter: 0.79
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

2,3,5,6-tetrahydroimidazo[2,1-b]thiazole
dichloromethaneN  Parameter: 12.98
sN Parameter: 0.81
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole
dichloromethaneN  Parameter: 13.42
sN Parameter: 0.73
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

2,3-dihydrofuran
dichloromethaneN  Parameter: 4.37
sN Parameter: 0.90
****Eur. J. Org. Chem. 2005, , 1760-1764
DOI: 10.1002/ejoc.200400706
image of molecule

2,3-dimethyl-but-1-ene
dichloromethaneN  Parameter: 0.65
sN Parameter: 1.00
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2,3-dimethyl-buta-1,3-diene
dichloromethaneN  Parameter: 1.17
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2,4,4-trimethyl-pent-1-ene
dichloromethaneN  Parameter: 0.79
sN Parameter: 1.07
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2,4,5-trimethyl-1,3-dioxolane (anti)
dichloromethaneN  Parameter: -3.00
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2,4,5-trimethyl-1,3-dioxolane (syn)
dichloromethaneN  Parameter: -2.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2,4,6-trimethylpyridine (in CH2Cl2)
dichloromethaneN  Parameter: 9.34
sN Parameter: 0.71
***Synthesis 2017, 49, 3495-3504
DOI: 10.1055/s-0036-1590504
image of molecule

2,4,6-trimethylpyridine (in MeCN)
MeCNN  Parameter: 9.39
sN Parameter: 0.60
***Synthesis 2017, 49, 3495-3504
DOI: 10.1055/s-0036-1590504
image of molecule

2,4,6-trimethylstyrene
dichloromethaneN  Parameter: 0.68
sN Parameter: 1.09
***Macromolecules 2005, 38, 33-40
DOI: 10.1021/ma048389o
image of molecule

2,4-dimethyl-imidazole (in MeCN)
MeCNN  Parameter: 11.51
sN Parameter: 0.84
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

2,4-dimethyl-imidazole anion (in DMSO)
DMSON  Parameter: 20.69
sN Parameter: 0.60
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

2,4-dimethyl-penta-1,4-diene
dichloromethaneN  Parameter: 0.54
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2,4-dimethylpyrrole
MeCNN  Parameter: 10.67
sN Parameter: 0.91
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092
image of molecule

2,5-dimethyl-benzimidazole (in DMSO)
DMSON  Parameter: 10.21
sN Parameter: 0.85
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

2,5-dimethyl-hexa-1,5-diene
dichloromethaneN  Parameter: 1.14
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2,5-dimethylindole
MeCNN  Parameter: 7.22
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

2,5-dimethylpyrrole
MeCNN  Parameter: 8.01
sN Parameter: 0.96
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092
image of molecule

2,6-dimethyl-hepta-1,6-diene
dichloromethaneN  Parameter: 1.69
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2,6-dimethylphenyl isocyanide
dichloromethaneN  Parameter: 4.59
sN Parameter: 0.87
***Angew. Chem. Int. Ed. 2007, 46, 3563-3566
DOI: 10.1002/anie.200605205
image of molecule

2,6-dimethylpyridine (in CH2Cl2)
dichloromethaneN  Parameter: 9.87
sN Parameter: 0.68
***Synthesis 2017, 49, 3495-3504
DOI: 10.1055/s-0036-1590504
image of molecule

2,6-dimethylpyridine (in MeCN)
MeCNN  Parameter: 9.11
sN Parameter: 0.69
***Synthesis 2017, 49, 3495-3504
DOI: 10.1055/s-0036-1590504
image of molecule

2,7-dimethylocta-1,7-diene
dichloromethaneN  Parameter: 1.58
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-((2,2,5,5-tetramethyl-1-(prop-1-en-1-yl)-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in MeCN)
MeCNN  Parameter: 9.25
sN Parameter: 0.84
***Chem. Commun. 2023, 59, 8091-8084
DOI: 10.1039/d3cc01912h
image of molecule

2-((2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in CH2Cl2)
dichloromethaneN  Parameter: 7.06
sN Parameter: 1.11
***Chem. Commun. 2023, 59, 8091-8084
DOI: 10.1039/d3cc01912h
image of molecule

2-((2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in MeCN)
MeCNN  Parameter: 7.74
sN Parameter: 0.87
***Chem. Commun. 2023, 59, 8091-8084
DOI: 10.1039/d3cc01912h
image of molecule

2-(3-chlorophenyl)-1,3-dimethyl-benzimidazoline (in MeCN)
MeCNN  Parameter: 9.38
sN Parameter: 0.71
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-(3-Cl-C6H4)CH(-)CO2Et (in DMSO)
DMSON  Parameter: 27.57
sN Parameter: 0.53
***Eur. J. Org. Chem. 2013, , 4255-4261
DOI: 10.1002/ejoc.201300265
image of molecule

2-(4-(trifluoromethyl)phenyl)-1,3-dimethyl-benzimidazoline (in MeCN)
MeCNN  Parameter: 8.74
sN Parameter: 0.71
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-(4-Br-C6H4)CH(-)CO2Et (in DMSO)
DMSON  Parameter: 27.62
sN Parameter: 0.53
***Eur. J. Org. Chem. 2013, , 4255-4261
DOI: 10.1002/ejoc.201300265
image of molecule

2-(4-CN-C6H4)CH(-)CO2Et (in DMSO)
DMSON  Parameter: 23.64
sN Parameter: 0.65
***Eur. J. Org. Chem. 2013, , 4255-4261
DOI: 10.1002/ejoc.201300265
image of molecule

2-(4-nitrophenyl)-1,3-dimethyl-benzimidazoline (in MeCN)
MeCNN  Parameter: 8.36
sN Parameter: 0.71
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-(4-NO2-C6H4)CH(-)CO2Et (in DMSO)
DMSON  Parameter: 20.00
sN Parameter: 0.71
***Eur. J. Org. Chem. 2013, , 4255-4261
DOI: 10.1002/ejoc.201300265
image of molecule

2-(benzylideneamino)-1-ethoxy-1-oxopropan-2-ide (in DMSO)
DMSON  Parameter: 30.82
sN Parameter: 0.41
**Tetrahedron 2019, 75, 459-463
DOI: 10.1016/j.tet.2018.11.075
image of molecule

2-(bis(tert-butyldimethylsiloxy)amino)propene
dichloromethaneN  Parameter: 4.23
sN Parameter: 0.93
***J. Org. Chem. 2001, 66, 3196-3200
DOI: 10.1021/jo0015927
image of molecule

2-(bis(trimethylsiloxy)amino)propene
dichloromethaneN  Parameter: 4.76
sN Parameter: 0.86
***J. Org. Chem. 2001, 66, 3196-3200
DOI: 10.1021/jo0015927
image of molecule

2-(diethylamino)-2-oxo-1-(pyridin-1-ium-1-yl)ethan-1-ide (in DMSO)
DMSON  Parameter: 27.45
sN Parameter: 0.38
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

2-(naphthylmethyl)quinuclidine (in MeCN)
MeCNN  Parameter: 15.66
sN Parameter: 0.62
***J. Org. Chem. 2009, 74, 7157-7164
DOI: 10.1021/jo901670w
image of molecule

2-(p-anisyl)-1,3-dimethyl-benzimidazoline
MeCNN  Parameter: 10.01
sN Parameter: 0.72
***Chem. Asian J. 2009, 4, 1824-1829
DOI: 10.1002/asia.200900322
image of molecule

2-(p-tolyl)-1,3-dimethyl-benzimidazoline
MeCNN  Parameter: 10.14
sN Parameter: 0.70
***Chem. Asian J. 2009, 4, 1824-1829
DOI: 10.1002/asia.200900322
image of molecule

2-(pentamethyldisilyl)propene
dichloromethaneN  Parameter: -0.26
sN Parameter: 0.95
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

2-(pyrid-4-yl)CH(-)CO2Et (in DMSO)
DMSON  Parameter: 23.27
sN Parameter: 0.70
***Eur. J. Org. Chem. 2013, , 4255-4261
DOI: 10.1002/ejoc.201300265
image of molecule

2-(tert-butoxy)-1-((diphenylmethylene)amino)-2-oxoethan-1-ide (in DMSO)
DMSON  Parameter: 27.77
sN Parameter: 0.47
***Tetrahedron 2019, 75, 459-463
DOI: 10.1016/j.tet.2018.11.075
image of molecule

2-(tert.butyldimethylsiloxy)propene
dichloromethaneN  Parameter: 5.58
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(tributylsilyl)furan
dichloromethaneN  Parameter: 2.37
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(tributylstannyl)furan
dichloromethaneN  Parameter: 3.63
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(tributylstannyl)thiophene
dichloromethaneN  Parameter: 1.53
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(triethylsilyl)furan
dichloromethaneN  Parameter: 2.20
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(trifluoromethyl)pyrrolidine
MeCNN  Parameter: 11.34
sN Parameter: 0.73
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

2-(triisopropylsiloxy)propene
dichloromethaneN  Parameter: 5.38
sN Parameter: 0.85
**J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-(trimethylsiloxy)-5,6-dihydro-4H-pyran
dichloromethaneN  Parameter: 10.61
sN Parameter: 0.86
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-(trimethylsiloxy)-5,6-dihydro-4H-pyran (in MeCN)
MeCNN  Parameter: 10.52
sN Parameter: 0.78
***J. Am. Chem. Soc. 2013, 135, 6579-6587
DOI: 10.1021/ja401106x
image of molecule

2-(trimethylsiloxy)buta-1,3-diene
dichloromethaneN  Parameter: 4.83
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(trimethylsiloxy)furan
dichloromethaneN  Parameter: 7.22
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(trimethylsiloxy)propene
dichloromethaneN  Parameter: 5.41
sN Parameter: 0.91
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-(trimethylsilyl)furan
dichloromethaneN  Parameter: 2.16
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(trimethylsilyl)propene
dichloromethaneN  Parameter: -1.46
sN Parameter: 1.05
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

2-(trimethylsilyl)thiophene
dichloromethaneN  Parameter: -0.80
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(triphenylsiloxy)propene
dichloromethaneN  Parameter: 4.46
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(triphenylsilyl)pyrrolidine
MeCNN  Parameter: 14.00
sN Parameter: 0.84
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

2-(tris(pentafluorophenyl)siloxy)-propene
dichloromethaneN  Parameter: 0.58
sN Parameter: 0.91
*Eur. J. Org. Chem. 2005, , 1760-1764
DOI: 10.1002/ejoc.200400706
image of molecule

2-(tris(trimethylsilyl)siloxy)propene
dichloromethaneN  Parameter: 6.04
sN Parameter: 0.82
***Org. Lett. 2010, 12, 5206-5209
DOI: 10.1021/ol102220e
image of molecule

2-(tris(trimethylsilyl)silyl)propene
dichloromethaneN  Parameter: -0.31
sN Parameter: 0.99
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

2-Ac super-dmap (in MeCN)
MeCNN  Parameter: 15.39
sN Parameter: 0.60
***Org. Lett. 2011, 13, 530-533
DOI: 10.1021/ol1029589
image of molecule

2-aminobutan-1-ol (in DMSO)
DMSON  Parameter: 14.39
sN Parameter: 0.67
***J. Am. Chem. Soc. 2009, 131, 11392-11401
DOI: 10.1021/ja903207b
image of molecule

2-benzyl-1,1,3,3-tetramethylguanidine
dichloromethaneN  Parameter: 14.36
sN Parameter: 0.79
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

2-benzylpyrrolidine
MeCNN  Parameter: 17.43
sN Parameter: 0.66
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

2-Bn super-dmap (in MeCN)
MeCNN  Parameter: 17.69
sN Parameter: 0.57
***Org. Lett. 2011, 13, 530-533
DOI: 10.1021/ol1029589
image of molecule

2-Bz super-dmap (in MeCN)
MeCNN  Parameter: 14.19
sN Parameter: 0.67
***Org. Lett. 2011, 13, 530-533
DOI: 10.1021/ol1029589
image of molecule

2-chloro-1,3-diethoxy-1,3-dioxopropan-2-ide (in DMSO)
DMSON  Parameter: 18.19
sN Parameter: 0.74
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

2-chloropropene
dichloromethaneN  Parameter: -3.65
sN Parameter: 1.97
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2-cyclopropylpropene
dichloromethaneN  Parameter: 2.60
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-diazo-1-benzosuberone
dichloromethaneN  Parameter: 2.72
sN Parameter: 0.96
***Eur. J. Org. Chem. 2023, 26, e202300005
DOI: 10.1002/ejoc.202300005
image of molecule

2-diazo-1-tetralone
dichloromethaneN  Parameter: 3.51
sN Parameter: 0.86
***Eur. J. Org. Chem. 2023, 26, e202300005
DOI: 10.1002/ejoc.202300005
image of molecule

2-diazobenzothiophen-3(2H)-one
dichloromethaneN  Parameter: 0.40
sN Parameter: 0.93
***Eur. J. Org. Chem. 2023, 26, e202300005
DOI: 10.1002/ejoc.202300005
image of molecule

2-diazocyclohexanone
dichloromethaneN  Parameter: 3.44
sN Parameter: 0.83
***Eur. J. Org. Chem. 2023, 26, e202300005
DOI: 10.1002/ejoc.202300005
image of molecule

2-diazoindan-1-one
dichloromethaneN  Parameter: 5.61
sN Parameter: 0.65
***Eur. J. Org. Chem. 2023, 26, e202300005
DOI: 10.1002/ejoc.202300005
image of molecule

2-diazoindandione
dichloromethaneN  Parameter: 0.16
sN Parameter: 0.86
***Eur. J. Org. Chem. 2023, 26, e202300005
DOI: 10.1002/ejoc.202300005
image of molecule

2-Et super-dmap (in MeCN)
MeCNN  Parameter: 16.81
sN Parameter: 0.60
***Org. Lett. 2011, 13, 530-533
DOI: 10.1021/ol1029589
image of molecule

2-ethoxy-1-fluoro-2-oxo-1-(phenylsulfonyl)ethan-1-ide (in DMSO)
DMSON  Parameter: 20.51
sN Parameter: 0.64
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

2-ethoxy-1-methoxy-2-oxo-1-(phenylsulfonyl)ethan-1-ide (in DMSO)
DMSON  Parameter: 19.15
sN Parameter: 0.59
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

2-ethoxy-2-oxo-1-(phenylsulfonyl)ethan-1-ide (in DMSO)
DMSON  Parameter: 18.81
sN Parameter: 0.59
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

2-ethoxy-2-oxo-1-(pyridin-1-ium-1-yl)ethan-1-ide (in DMSO)
DMSON  Parameter: 26.71
sN Parameter: 0.37
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

2-ethyl-4,5-dimethyl-1,3-dioxolane (anti)
dichloromethaneN  Parameter: -2.90
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-ethyl-4,5-dimethyl-1,3-dioxolane (syn)
dichloromethaneN  Parameter: -2.40
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-fluoro-2H-benzo[d][1,3]dithiol-2-ide 1,1,3,3-tetraoxide (in DMSO)
DMSON  Parameter: 19.03
sN Parameter: 0.58
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

2-formyl-imidazole anion (in DMSO)
DMSON  Parameter: 16.06
sN Parameter: 0.68
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

2-formyl-imidazole anion (in water)
waterN  Parameter: 11.07
sN Parameter: 0.50
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

2-isopropyl-4,5-dimethyl-1,3-dioxolane (ani)
dichloromethaneN  Parameter: -4.10
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-isopropyl-4,5-dimethyl-1,3-dioxolane (syn)
dichloromethaneN  Parameter: -3.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-Me super-dmap (in MeCN)
MeCNN  Parameter: 16.65
sN Parameter: 0.58
***Org. Lett. 2011, 13, 530-533
DOI: 10.1021/ol1029589
image of molecule

2-methoxy-2H-benzo[d][1,3]dithiol-2-ide 1,1,3,3-tetraoxide (in DMSO)
DMSON  Parameter: 17.36
sN Parameter: 0.71
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

2-methyl-1,3-dioxolane
dichloromethaneN  Parameter: -3.30
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-methyl-1,4,5,6-tetrahydropyrimidine (in CH2Cl2)
dichloromethaneN  Parameter: 15.21
sN Parameter: 0.69
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-methyl-1,4,5,6-tetrahydropyrimidine (in DMSO)
DMSON  Parameter: 14.58
sN Parameter: 0.79
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-methyl-1,4,5,6-tetrahydropyrimidine (in MeCN)
MeCNN  Parameter: 14.43
sN Parameter: 0.79
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-methyl-1-(trimethylsiloxy)propen
dichloromethaneN  Parameter: 3.94
sN Parameter: 1.00
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-methyl-4,5-dihydro-1,3-oxazole (in CH2Cl2)
dichloromethaneN  Parameter: 9.81
sN Parameter: 0.77
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-methyl-4,5-dihydro-1H-imidazole (in CH2Cl2)
dichloromethaneN  Parameter: 12.92
sN Parameter: 0.77
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-methyl-4,5-dihydro-3H-pyrrole (in CH2Cl2)
dichloromethaneN  Parameter: 13.12
sN Parameter: 0.69
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-methyl-4,5-dihydrothiazole (in CH2Cl2)
dichloromethaneN  Parameter: 10.20
sN Parameter: 0.71
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-methyl-benzimidazole (in DMSO)
DMSON  Parameter: 10.02
sN Parameter: 0.85
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

2-methyl-but-1-ene
dichloromethaneN  Parameter: 1.00
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-methyl-but-2-ene
dichloromethaneN  Parameter: 0.65
sN Parameter: 1.17
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-methyl-buta-1,3-diene (isoprene)
dichloromethaneN  Parameter: 1.10
sN Parameter: 0.98
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-methyl-imidazole (in MeCN)
MeCNN  Parameter: 11.74
sN Parameter: 0.76
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

2-methyl-imidazole (in water)
waterN  Parameter: 9.45
sN Parameter: 0.54
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

2-methyl-imidazole anion (in DMSO)
DMSON  Parameter: 21.03
sN Parameter: 0.50
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

2-methyl-pent-1-ene
dichloromethaneN  Parameter: 0.84
sN Parameter: 1.06
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2-methylfuran
dichloromethaneN  Parameter: 3.61
sN Parameter: 1.11
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-methylindole
MeCNN  Parameter: 6.91
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

2-methylpropene (isobutylene)
dichloromethaneN  Parameter: 1.11
sN Parameter: 0.98
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-methylpyridine (in CH2Cl2)
dichloromethaneN  Parameter: 10.52
sN Parameter: 0.78
***Synthesis 2017, 49, 3495-3504
DOI: 10.1055/s-0036-1590504
image of molecule

2-methylpyridine (in MeCN)
MeCNN  Parameter: 10.98
sN Parameter: 0.66
***Synthesis 2017, 49, 3495-3504
DOI: 10.1055/s-0036-1590504
image of molecule

2-methylpyrrolidine (in MeCN)
MeCNN  Parameter: 16.78
sN Parameter: 0.71
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

2-methylthiophene
dichloromethaneN  Parameter: 1.35
sN Parameter: 0.99
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2-oxo-1-(pyridin-1-ium-1-yl)propan-1-ide (in DMSO)
DMSON  Parameter: 20.24
sN Parameter: 0.60
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

2-oxo-2-phenyl-1-(pyridin-1-ium-1-yl)ethan-1-ide (in DMSO)
DMSON  Parameter: 19.46
sN Parameter: 0.58
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

2-oxo-2-phenyl-1-(quinolin-1-ium-1-yl)ethan-1-ide (in DMSO)
DMSON  Parameter: 19.38
sN Parameter: 0.50
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

2-PhCH(-)CO2Et (in DMSO)
DMSON  Parameter: 27.54
sN Parameter: 0.57
***Eur. J. Org. Chem. 2013, , 4255-4261
DOI: 10.1002/ejoc.201300265
image of molecule

2-phenyl-1,3-dimethyl-benzimidazoline
MeCNN  Parameter: 9.72
sN Parameter: 0.72
***Chem. Asian J. 2009, 4, 1824-1829
DOI: 10.1002/asia.200900322
image of molecule

2-phenyl-1,4,5,6-tetrahydropyrimidine (in CH2Cl2)
dichloromethaneN  Parameter: 14.62
sN Parameter: 0.72
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-phenyl-4,5-dihydro-1H-imidazole (in CH2Cl2)
dichloromethaneN  Parameter: 12.31
sN Parameter: 0.77
***Eur. J. Org. Chem. 2013, , 3369-3377
DOI: 10.1002/ejoc.201300213
image of molecule

2-phenyl-4-(trimethylsilyl)but-1-en-3-ynyl-Co2(CO)6
dichloromethaneN  Parameter: 1.33
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-phenyl-allyltrimethylsilane
dichloromethaneN  Parameter: 5.38
sN Parameter: 0.89
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

2-phenyldioxolane
dichloromethaneN  Parameter: -0.90
sN Parameter: 0.80
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-phenylethylamine (in water)
waterN  Parameter: 13.40
sN Parameter: 0.57
***ChemPlusChem 2015, 80, 1673-1679
DOI: 10.1002/cplu.201500246
image of molecule

2-phenylperoxyacetate (in H2O)
waterN  Parameter: 15.63
sN Parameter: 0.56
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

2-propyl-1,3-dioxolane
dichloromethaneN  Parameter: -1.06
sN Parameter: 0.81
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

2-pyridone anion (in DMSO)
DMSON  Parameter: 19.91
sN Parameter: 0.60
***J. Am. Chem. Soc. 2010, 132, 15380-15389
DOI: 10.1021/ja106962u
image of molecule

2-pyridone anion (in MeCN)
MeCNN  Parameter: 20.11
sN Parameter: 0.57
***J. Am. Chem. Soc. 2010, 132, 15380-15389
DOI: 10.1021/ja106962u
image of molecule

2-pyridone anion (in water)
waterN  Parameter: 12.47
sN Parameter: 0.52
***J. Am. Chem. Soc. 2010, 132, 15380-15389
DOI: 10.1021/ja106962u
image of molecule

2-sulfidoacetate (in water)
waterN  Parameter: 22.62
sN Parameter: 0.43
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

2-thiobarbiturate anion (in DMSO)
DMSON  Parameter: 14.24
sN Parameter: 0.82
***J. Org. Chem. 2017, 82, 8476-8488
DOI: 10.1021/acs.joc.7b01223
image of molecule

2-tritylpyrrolidine
MeCNN  Parameter: 9.16
sN Parameter: 1.39
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

20% ethanol/80% MeCN (v/v)
EtOH-MeCN mixN  Parameter: 5.77
sN Parameter: 0.92
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

20% methanol/80% MeCN (v/v)
MeOH-MeCN mixN  Parameter: 6.04
sN Parameter: 0.94
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

20% water/80% acetone (v/v)
water-acetone mixN  Parameter: 5.77
sN Parameter: 0.87
***Angew. Chem. Int. Ed. 2004, 43, 2302-2305
DOI: 10.1002/anie.200353468
image of molecule

20% water/80% MeCN (v/v)
water-MeCN mixN  Parameter: 5.02
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

20% water/80%EtOH (v/v)
water-EtOH mixN  Parameter: 6.68
sN Parameter: 0.85
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

20% water/80%TFE (v/v)
water-TFE mixN  Parameter: 3.20
sN Parameter: 0.88
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

2H-benzo[d][1,3]dithiol-2-ide 1,1,3,3-tetraoxide (in DMSO)
DMSON  Parameter: 16.06
sN Parameter: 0.69
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

3% water/97% HFIP (w/w)
water-HFIP mixN  Parameter: -1.19
sN Parameter: 1.08
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

3,3,3-trifluoro-2-(trimethylsiloxy)propene
dichloromethaneN  Parameter: -2.94
sN Parameter: 1.11
***Org. Lett. 2012, 14, 3990-3993
DOI: 10.1021/ol301766w
image of molecule

3,3-dimethyl-2-(trimethylsiloxy)buten
dichloromethaneN  Parameter: 3.78
sN Parameter: 0.79
**J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

3,5,6,7-tetrahydro-2H-imidazo[2,1-b][1,3]thiazine
dichloromethaneN  Parameter: 13.00
sN Parameter: 0.83
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

3,5-bis(trifluoromethyl)thiophenolate (in DMSO)
DMSON  Parameter: 19.71
sN Parameter: 0.86
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

3,5-dichloroperoxybenzoate (in H2O)
waterN  Parameter: 17.93
sN Parameter: 0.50
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

3,5-dinitrobenzoate (in acetone)
acetoneN  Parameter: 18.80
sN Parameter: 0.62
**J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

3,5-dinitrobenzoate (in MeCN)
MeCNN  Parameter: 14.90
sN Parameter: 0.71
**J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

3-(2,6-dimethoxyphenyl)-1-methyl-1H-imidazol-3-ium-2-ide (in THF)
THFN  Parameter: 23.00
sN Parameter: 0.46
***Org. Lett. 2016, 18, 3566-3569
DOI: 10.1021/acs.orglett.6b01525
image of molecule

3-(4-methoxyphenyl)-1-methyl-1H-imidazol-3-ium-2-ide (in THF)
THFN  Parameter: 20.41
sN Parameter: 0.46
***Org. Lett. 2016, 18, 3566-3569
DOI: 10.1021/acs.orglett.6b01525
image of molecule

3-(tert-butyl)-1-methyl-1H-imidazol-3-ium-2-ide (in THF)
THFN  Parameter: 16.54
sN Parameter: 0.47
***Org. Lett. 2016, 18, 3566-3569
DOI: 10.1021/acs.orglett.6b01525
image of molecule

3-(trifluoromethyl)thiophenolate (in DMSO)
DMSON  Parameter: 21.75
sN Parameter: 0.86
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

3-(trihexylsilyl)cyclopentene
dichloromethaneN  Parameter: 1.98
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

3-(trimethylsiloxy)-1H-indene (in MeCN)
MeCNN  Parameter: 7.32
sN Parameter: 0.82
***Synthesis 2019, 51, 1157-1170
DOI: 10.1055/s-0037-1611634
image of molecule

3-(trimethylsilyl)cyclopentene
dichloromethaneN  Parameter: 1.77
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

3-acetyl-2-oxotetrahydro-2H-pyran-3-ide (in DMSO)
DMSON  Parameter: 17.00
sN Parameter: 0.74
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

3-bromo-4-(dimethylamino)pyridine (in MeCN)
MeCNN  Parameter: 12.96
sN Parameter: 0.67
***J. Phys. Chem. A 2012, 116, 8494-8499
DOI: 10.1021/jp3049247
image of molecule

3-chloro-4-methoxyperoxybenzoate (in H2O)
waterN  Parameter: 18.56
sN Parameter: 0.48
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

3-chloroperoxybenzoate (in H2O)
waterN  Parameter: 18.19
sN Parameter: 0.47
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

3-chlorothiophenolate (in DMSO)
DMSON  Parameter: 22.50
sN Parameter: 0.78
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

3-diazoindolin-2-one
dichloromethaneN  Parameter: 3.16
sN Parameter: 1.03
***Eur. J. Org. Chem. 2023, 26, e202300005
DOI: 10.1002/ejoc.202300005
image of molecule

3-ethyl-2,4-dimethylpyrrole
MeCNN  Parameter: 11.63
sN Parameter: 0.95
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092
image of molecule

3-mesityl-1-methyl-1H-imidazol-3-ium-2-ide (in THF)
THFN  Parameter: 21.50
sN Parameter: 0.45
***Org. Lett. 2016, 18, 3566-3569
DOI: 10.1021/acs.orglett.6b01525
image of molecule

3-methoxythiophene
MeCNN  Parameter: 3.06
sN Parameter: 1.19
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

3-methyl-1,4-pentadiene
dichloromethaneN  Parameter: -3.08
sN Parameter: 0.97
*J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

3-methyl-2,4-dioxotetrahydro-2H-pyran-3-ide (in DMSO)
DMSON  Parameter: 14.46
sN Parameter: 0.91
***Eur. J. Org. Chem. 2015, , 7594-7601
DOI: 10.1002/ejoc.201501107
image of molecule

3-methyl-2-(trimethylsiloxy)but-1-ene
dichloromethaneN  Parameter: 5.41
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

3-methylanisole
dichloromethaneN  Parameter: 0.13
sN Parameter: 1.27
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

3-methylpyridine (in CH2Cl2)
dichloromethaneN  Parameter: 10.90
sN Parameter: 0.93
***J. Phys. Org. Chem. 2016, 29, 759-767
DOI: 10.1002/poc.3580
image of molecule

3-methylpyridine (in MeCN)
MeCNN  Parameter: 11.50
sN Parameter: 0.80
***J. Phys. Org. Chem. 2016, 29, 759-767
DOI: 10.1002/poc.3580
image of molecule

3-propylcyclopentene
dichloromethaneN  Parameter: -0.88
sN Parameter: 0.94
***J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

3-pyrrolidino-1H-indene (in MeCN)
MeCNN  Parameter: 15.27
sN Parameter: 0.93
***Synthesis 2019, 51, 1157-1170
DOI: 10.1055/s-0037-1611634
image of molecule

30% water/70% HFIP (w/w)
water-HFIP mixN  Parameter: 1.65
sN Parameter: 0.96
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

33% ethanol/67% MeCN (v/v)
EtOH-MeCN mixN  Parameter: 6.06
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

33% methanol/67% MeCN (v/v)
MeOH-MeCN mixN  Parameter: 6.38
sN Parameter: 0.92
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

33% water/67% MeCN (v/v)
water-MeCN mixN  Parameter: 5.02
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane (in CH2Cl2)
dichloromethaneN  Parameter: -0.64
sN Parameter: 1.10
***J. Am. Chem. Soc. 2017, 139, 15324-15327
DOI: 10.1021/jacs.7b10240
image of molecule

4,4-dimethyl-glutarimide anion (in DMSO)
DMSON  Parameter: 17.52
sN Parameter: 0.63
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

4,5-dimethyl-1,3-dioxolane (anti)
dichloromethaneN  Parameter: -2.40
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

4,5-dimethyl-2-vinyl-1,3-dioxolane
dichloromethaneN  Parameter: -2.60
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

4-(2-(fluorodiphenylmethyl)pyrrolidin-1-yl)pyridine
dichloromethaneN  Parameter: 14.57
sN Parameter: 0.75
***Eur. J. Org. Chem. 2014, , 1202-1211
DOI: 10.1002/ejoc.201301730
image of molecule

4-(bis(trimethylsiloxy)amino)pent-4-enoic acid methyl ester
dichloromethaneN  Parameter: 3.84
sN Parameter: 0.87
***J. Org. Chem. 2001, 66, 3196-3200
DOI: 10.1021/jo0015927
image of molecule

4-(dimethylamino)pyridine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.20
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-(dimethylamino)pyridine (in CH2Cl2)
dichloromethaneN  Parameter: 15.80
sN Parameter: 0.66
***Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-(dimethylamino)pyridine (in DMF)
DMFN  Parameter: 14.90
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-(dimethylamino)pyridine (in DMSO)
DMSON  Parameter: 14.80
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-(dimethylamino)pyridine (in H2O)
waterN  Parameter: 13.19
sN Parameter: 0.56
***Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-(dimethylamino)pyridine (in MeCN)
MeCNN  Parameter: 15.51
sN Parameter: 0.62
***J. Phys. Chem. A 2012, 116, 8494-8499
DOI: 10.1021/jp3049247
image of molecule

4-(dimethylamino)pyridine (in THF)
THFN  Parameter: 15.90
sN Parameter: 0.66
***Angew. Chem. Int. Ed. 2011, 50, 6915-6919
DOI: 10.1002/anie.201102435
image of molecule

4-(morpholino)pyridine (in CH2Cl2)
dichloromethaneN  Parameter: 14.59
sN Parameter: 0.69
***Eur. J. Org. Chem. 2016, , 4050-4058
DOI: 10.1002/ejoc.201600572
image of molecule

4-(morpholino)pyridine (in MeCN)
MeCNN  Parameter: 14.80
sN Parameter: 0.63
***J. Phys. Chem. A 2012, 116, 8494-8499
DOI: 10.1021/jp3049247
image of molecule

4-(trifluoromethyl)thiophenolate (in DMSO)
DMSON  Parameter: 21.30
sN Parameter: 0.86
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

4-(trimethylsilyl)but-1-en-3-ynyl-Co2(CO)5(PPh3)
dichloromethaneN  Parameter: -0.76
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

4-(trimethylsilyl)but-1-en-3-ynyl-Co2(CO)6
dichloromethaneN  Parameter: -1.11
sN Parameter: 0.92
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

4-acetamido-pyridine (in MeCN)
MeCNN  Parameter: 13.24
sN Parameter: 0.67
***J. Phys. Chem. A 2012, 116, 8494-8499
DOI: 10.1021/jp3049247
image of molecule

4-amino-3,5-dibromo-pyridine (in MeCN)
MeCNN  Parameter: 11.11
sN Parameter: 0.75
***J. Phys. Chem. A 2012, 116, 8494-8499
DOI: 10.1021/jp3049247
image of molecule

4-aminopyridine (in CH2Cl2)
dichloromethaneN  Parameter: 15.20
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-aminopyridine (in H2O)
waterN  Parameter: 12.19
sN Parameter: 0.66
***Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-bromothiophenolate (in DMSO)
DMSON  Parameter: 22.80
sN Parameter: 0.78
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

4-chloroaniline (in MeCN)
MeCNN  Parameter: 12.92
sN Parameter: 0.60
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

4-chloropyridine (in CH2Cl2)
dichloromethaneN  Parameter: 11.70
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-chloropyridine (in H2O)
waterN  Parameter: 10.50
sN Parameter: 0.73
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-cyanophenyl isocyanide
dichloromethaneN  Parameter: 3.57
sN Parameter: 0.72
**Angew. Chem. Int. Ed. 2007, 46, 3563-3566
DOI: 10.1002/anie.200605205
image of molecule

4-fluoroperoxybenzoate (in H2O)
waterN  Parameter: 17.99
sN Parameter: 0.47
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

4-formyl-imidazole anion (in DMSO)
DMSON  Parameter: 16.40
sN Parameter: 0.67
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

4-methoxy-indole
MeCNN  Parameter: 5.41
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

4-methoxyaniline (in MeCN)
MeCNN  Parameter: 13.42
sN Parameter: 0.73
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

4-methoxyaniline (in water)
waterN  Parameter: 14.28
sN Parameter: 0.68
***ChemPlusChem 2015, 80, 1673-1679
DOI: 10.1002/cplu.201500246
image of molecule

4-methoxyperoxybenzoate (in H2O)
waterN  Parameter: 17.84
sN Parameter: 0.46
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

4-methoxypyridine (in CH2Cl2)
dichloromethaneN  Parameter: 13.70
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-methoxypyridine (in H2O)
waterN  Parameter: 11.44
sN Parameter: 0.68
***Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-methoxythiophenolate (in DMSO)
DMSON  Parameter: 24.97
sN Parameter: 0.68
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

4-methyl-2,5-heptadiene
dichloromethaneN  Parameter: -0.73
sN Parameter: 0.97
*J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

4-methyl-5-(trimethylsiloxy)-2,3-dihydrofuran
dichloromethaneN  Parameter: 11.50
sN Parameter: 0.91
***Eur. J. Org. Chem. 2004, , 2791-2796
DOI: 10.1002/ejoc.200400134
image of molecule

4-methyl-imidazole (in MeCN)
MeCNN  Parameter: 11.79
sN Parameter: 0.77
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

4-methyl-imidazole anion (in DMSO)
DMSON  Parameter: 21.29
sN Parameter: 0.51
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

4-methyl-N-(2-phenylethynyl)-N-(phenylmethyl)benzenesulfonamide
dichloromethaneN  Parameter: 3.85
sN Parameter: 0.84
***Angew. Chem. Int. Ed. 2014, 53, 4968-4971
DOI: 10.1002/anie.201402055
image of molecule

4-methyl-penta-1,3-diene
dichloromethaneN  Parameter: 2.60
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

4-methyl-quinoline alias lepidine (in MeCN)
MeCNN  Parameter: 11.60
sN Parameter: 0.62
***J. Org. Chem. 2009, 74, 7157-7164
DOI: 10.1021/jo901670w
image of molecule

4-methylpiperazin-1-yl dithiocarbamate (in MeCN)
MeCNN  Parameter: 23.61
sN Parameter: 0.57
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

4-methylpyridine (in CH2Cl2)
dichloromethaneN  Parameter: 13.70
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-methylpyridine (in H2O)
waterN  Parameter: 11.10
sN Parameter: 0.75
***Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-methylthiophenolate (in DMSO)
DMSON  Parameter: 24.35
sN Parameter: 0.69
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

4-nitro-imidazole anion (in DMSO)
DMSON  Parameter: 14.81
sN Parameter: 0.71
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

4-nitro-imidazole anion (in water)
waterN  Parameter: 11.37
sN Parameter: 0.53
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

4-nitroperoxybenzoate (in H2O)
waterN  Parameter: 17.43
sN Parameter: 0.50
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

4-nitrothiophenolate (in DMSO)
DMSON  Parameter: 18.92
sN Parameter: 0.87
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

4-pyridone anion (in DMSO)
DMSON  Parameter: 18.97
sN Parameter: 0.62
***J. Am. Chem. Soc. 2010, 132, 15380-15389
DOI: 10.1021/ja106962u
image of molecule

4-pyridone anion (in MeCN)
MeCNN  Parameter: 20.22
sN Parameter: 0.49
***J. Am. Chem. Soc. 2010, 132, 15380-15389
DOI: 10.1021/ja106962u
image of molecule

4-pyridone anion (in water)
waterN  Parameter: 14.76
sN Parameter: 0.48
***J. Am. Chem. Soc. 2010, 132, 15380-15389
DOI: 10.1021/ja106962u
image of molecule

4-pyrrolidinopyridine (in CH2Cl2)
dichloromethaneN  Parameter: 15.90
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-pyrrolidinopyridine (in H2O)
waterN  Parameter: 12.39
sN Parameter: 0.66
***Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

4-pyrrolidinopyridine (in MeCN)
MeCNN  Parameter: 14.99
sN Parameter: 0.69
***Chem. Eur. J. 2013, 19, 6435-6442
DOI: 10.1002/chem.201204452
image of molecule

40% water/60%EtOH (v/v)
water-EtOH mixN  Parameter: 6.28
sN Parameter: 0.87
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

40% water/60%TFE (v/v)
water-TFE mixN  Parameter: 3.42
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

5% water/95% HFIP (w/w)
water-HFIP mixN  Parameter: -0.10
sN Parameter: 0.97
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

5,6-dimethyl-benzimidazole (in DMSO)
DMSON  Parameter: 11.08
sN Parameter: 0.71
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

5-(4-(dimethylamino)benzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide
MeCNN  Parameter: 7.15
sN Parameter: 0.81
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

5-(4-(dimethylamino)benzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)
DMSON  Parameter: 14.48
sN Parameter: 0.86
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

5-(4-(methoxy)benzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide
MeCNN  Parameter: 6.21
sN Parameter: 0.68
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

5-(4-(methoxy)benzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)
DMSON  Parameter: 15.13
sN Parameter: 0.75
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

5-(4-cyanobenzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)
DMSON  Parameter: 13.79
sN Parameter: 0.86
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

5-(tert-Butyl)-1,3-diisopropyl-4-methylene-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)
THFN  Parameter: 31.92
sN Parameter: 0.52
***Angew. Chem. Int. Ed. 2023, 62, e202309790
DOI: 10.1002/anie.202309790
image of molecule

5-(trimethylsiloxy)-2,3-dihydrofuran
dichloromethaneN  Parameter: 12.56
sN Parameter: 0.70
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

5-(trimethylsiloxy)-2,3-dihydrofuran (in MeCN)
MeCNN  Parameter: 12.34
sN Parameter: 0.72
***J. Am. Chem. Soc. 2013, 135, 6579-6587
DOI: 10.1021/ja401106x
image of molecule

5-(triphenylsiloxy)-2,3-dihydrofuran
dichloromethaneN  Parameter: 11.28
sN Parameter: 0.91
***Eur. J. Org. Chem. 2005, , 1760-1764
DOI: 10.1002/ejoc.200400706
image of molecule

5-(tris(pentafluorophenyl)siloxy)-2,3-dihydrofuran
dichloromethaneN  Parameter: 8.16
sN Parameter: 0.67
***Eur. J. Org. Chem. 2005, , 1760-1764
DOI: 10.1002/ejoc.200400706
image of molecule

5-amino-indole
MeCNN  Parameter: 7.22
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-benzyl-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide
MeCNN  Parameter: 5.51
sN Parameter: 0.70
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

5-benzyl-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)
DMSON  Parameter: 15.02
sN Parameter: 0.75
***Chem. Eur. J. 2014, 20, 11069-11077
DOI: 10.1002/chem.201403161
image of molecule

5-bromo-indole
MeCNN  Parameter: 4.38
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-chloro-2-methylindole
MeCNN  Parameter: 6.08
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-chloro-indole
MeCNN  Parameter: 4.42
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-cyano-indole
MeCNN  Parameter: 2.83
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-hydroxy-indole
MeCNN  Parameter: 6.44
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-methoxy-2-methylindole
MeCNN  Parameter: 7.26
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-methoxy-benzimidazole (in DMSO)
DMSON  Parameter: 11.00
sN Parameter: 0.71
*Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

5-methoxy-indole
dichloromethaneN  Parameter: 6.22
sN Parameter: 1.12
***J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-methyl-benzimidazole (in DMSO)
DMSON  Parameter: 10.69
sN Parameter: 0.79
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

5-methyl-indole
MeCNN  Parameter: 6.00
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

50% ethanol/50% MeCN (v/v)
EtOH-MeCN mixN  Parameter: 6.37
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

50% methanol/50% MeCN (v/v)
MeOH-MeCN mixN  Parameter: 6.67
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

50% water/50% HFIP (w/w)
water-HFIP mixN  Parameter: 1.50
sN Parameter: 1.03
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

50% water/50% MeCN (v/v)
water-MeCN mixN  Parameter: 5.05
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

50% water/50%EtOH (v/v)
water-EtOH mixN  Parameter: 5.96
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

50% water/50%TFE (v/v)
water-TFE mixN  Parameter: 3.57
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

6,6-dimethylfulvene
MeCNN  Parameter: 3.93
sN Parameter: 0.88
***Eur. J. Org. Chem. 2009, , 1202-1206
DOI: 10.1002/ejoc.200801099
image of molecule

6-(4-dimethylamino-phenyl)fulvene
MeCNN  Parameter: 6.72
sN Parameter: 0.87
***Eur. J. Org. Chem. 2009, , 1202-1206
DOI: 10.1002/ejoc.200801099
image of molecule

6-(julolidin-9-yl)fulvene
MeCNN  Parameter: 7.79
sN Parameter: 1.06
***Eur. J. Org. Chem. 2009, , 1202-1206
DOI: 10.1002/ejoc.200801099
image of molecule

6-methoxy-quinoline (in MeCN)
MeCNN  Parameter: 10.86
sN Parameter: 0.66
***J. Org. Chem. 2009, 74, 7157-7164
DOI: 10.1021/jo901670w
image of molecule

6-methyl-3-(phenyl-l3-iodanylidene)dihydro-2H-pyran-2,4(3H)-dione (in CH2Cl2)
dichloromethaneN  Parameter: 4.67
sN Parameter: 0.92
***J. Am. Chem. Soc. 2016, 138, 10304-10313
DOI: 10.1021/jacs.6b05768
image of molecule

60% water/40%EtOH (v/v)
water-EtOH mixN  Parameter: 5.81
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

60% water/40%TFE (v/v)
water-TFE mixN  Parameter: 3.77
sN Parameter: 0.88
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

67% ethanol/33% MeCN (v/v)
EtOH-MeCN mixN  Parameter: 6.74
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

67% methanol/33% MeCN (v/v)
MeOH-MeCN mixN  Parameter: 7.01
sN Parameter: 0.91
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

67% water/33% MeCN (v/v)
water-MeCN mixN  Parameter: 5.05
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

7% water/93% HFIP (w/w)
water-HFIP mixN  Parameter: 0.34
sN Parameter: 0.96
***J. Phys. Org. Chem. 2013, 26, 59-63
DOI: 10.1002/poc.3064
image of molecule

7-azaindole
MeCNN  Parameter: 3.87
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

80% ethanol/20% MeCN (v/v)
EtOH-MeCN mixN  Parameter: 6.94
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

80% methanol/20% MeCN (v/v)
MeOH-MeCN mixN  Parameter: 7.20
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

80% water/20% MeCN (v/v)
water-MeCN mixN  Parameter: 5.04
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

80% water/20%EtOH (v/v)
water-EtOH mixN  Parameter: 5.54
sN Parameter: 0.94
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

80% water/20%TFE (v/v)
water-TFE mixN  Parameter: 4.78
sN Parameter: 0.83
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

9,10-dihydroanthracene
dichloromethaneN  Parameter: -0.86
sN Parameter: 0.92
***J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

9-methyl guanine anion (in water)
waterN  Parameter: 10.77
sN Parameter: 0.65
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

90% water/10%EtOH (v/v)
water-EtOH mixN  Parameter: 5.38
sN Parameter: 0.91
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

90% water/10%TFE (v/v)
water-TFE mixN  Parameter: 5.04
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

91% ethanol/9% MeCN (v/v)
EtOH-MeCN mixN  Parameter: 7.10
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

91% methanol/9% MeCN (v/v)
MeOH-MeCN mixN  Parameter: 7.45
sN Parameter: 0.87
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

91% n-propanol/9% MeCN (v/v)
nPrOH-MeCN mixN  Parameter: 7.05
sN Parameter: 0.80
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

91% propan-2-ol/9% MeCN (v/v)
iPrOH-MeCN mixN  Parameter: 6.49
sN Parameter: 0.96
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

91% water/9% MeCN (v/v)
water-MeCN mixN  Parameter: 5.16
sN Parameter: 0.91
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

acetate (in 80A20W)
aq acetoneN  Parameter: 12.50
sN Parameter: 0.60
**J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

acetate (in 90A10W)
aq acetoneN  Parameter: 12.71
sN Parameter: 0.68
***J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

acetate (in MeCN)
MeCNN  Parameter: 16.90
sN Parameter: 0.75
***J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

acetonitrile (in MeCN)
MeCNN  Parameter: 2.23
sN Parameter: 0.84
***J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

adenine anion (in DMSO)
DMSON  Parameter: 18.00
sN Parameter: 0.55
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

adenine anion (in water)
waterN  Parameter: 10.93
sN Parameter: 0.62
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

alanine (anionic, in water)
waterN  Parameter: 13.01
sN Parameter: 0.58
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

allyl-tert.butyl-dimethylsilane
dichloromethaneN  Parameter: 1.80
sN Parameter: 0.95
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

allylamine (in MeCN)
MeCNN  Parameter: 14.37
sN Parameter: 0.66
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

allylamine (in water)
waterN  Parameter: 13.21
sN Parameter: 0.54
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

allylbenzene
dichloromethaneN  Parameter: -4.12
sN Parameter: 0.97
*J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

allylchlorodimethylsilane
dichloromethaneN  Parameter: -0.57
sN Parameter: 1.06
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

allyltri-n-butylsilane
dichloromethaneN  Parameter: 2.09
sN Parameter: 0.95
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

allyltributylstannane
dichloromethaneN  Parameter: 5.46
sN Parameter: 0.89
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

allyltriethylsilane
dichloromethaneN  Parameter: 1.93
sN Parameter: 0.95
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

allyltrihexylsilane
dichloromethaneN  Parameter: 2.11
sN Parameter: 0.95
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

allyltriisopropylsilane
dichloromethaneN  Parameter: 2.04
sN Parameter: 0.95
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

allyltrimethylsilane
dichloromethaneN  Parameter: 1.68
sN Parameter: 1.00
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

allyltriphenylgermane
dichloromethaneN  Parameter: 1.20
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

allyltriphenylsilane
dichloromethaneN  Parameter: -0.13
sN Parameter: 1.21
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

allyltriphenylstannane
dichloromethaneN  Parameter: 3.09
sN Parameter: 0.90
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

allyltris(trimethylsilyl)silane
dichloromethaneN  Parameter: 1.95
sN Parameter: 0.98
***Org. Lett. 2010, 12, 5206-5209
DOI: 10.1021/ol102220e
image of molecule

alpha-(N-morpholino)styrene
dichloromethaneN  Parameter: 9.96
sN Parameter: 0.79
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

alpha-(N-morpholino)styrene (in MeCN)
MeCNN  Parameter: 10.30
sN Parameter: 0.80
*Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
image of molecule

alpha-(N-piperidino)styrene (in MeCN)
MeCNN  Parameter: 11.60
sN Parameter: 0.80
*Chem. Eur. J. 2018, 24, 5901-5910
DOI: 10.1002/chem.201705962
image of molecule

alpha-(pentamethyldisilyl)styrene
dichloromethaneN  Parameter: 0.61
sN Parameter: 1.01
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

alpha-(trimethylsilyl)styrene
dichloromethaneN  Parameter: -1.13
sN Parameter: 1.46
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

alpha-methylstyrene
dichloromethaneN  Parameter: 2.35
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

ammonia (in MeCN)
MeCNN  Parameter: 11.39
sN Parameter: 0.69
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

ammonia (in water)
waterN  Parameter: 9.48
sN Parameter: 0.59
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

aniline (in MeCN)
MeCNN  Parameter: 12.64
sN Parameter: 0.68
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

aniline (in water)
waterN  Parameter: 12.99
sN Parameter: 0.73
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

anion of (3-nitrophenyl)nitromethane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 14.75
sN Parameter: 0.71
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of (3-nitrophenyl)nitromethane (in DMSO)
DMSON  Parameter: 18.06
sN Parameter: 0.71
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of (3-nitrophenyl)nitromethane (in water)
waterN  Parameter: 14.25
sN Parameter: 0.46
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of (4-CF3-C6H4)CH2SO2Ph (in DMSO)
DMSON  Parameter: 24.30
sN Parameter: 0.51
***Org. Biomol. Chem. 2008, 6, 3052-3058
DOI: 10.1039/b805604h
image of molecule

anion of (4-CN-C6H4)CH2SO2Ph (in DMSO)
DMSON  Parameter: 22.60
sN Parameter: 0.57
***Org. Biomol. Chem. 2008, 6, 3052-3058
DOI: 10.1039/b805604h
image of molecule

anion of (4-cyanophenyl)nitromethane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.92
sN Parameter: 0.74
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of (4-cyanophenyl)nitromethane (in DMSO)
DMSON  Parameter: 16.96
sN Parameter: 0.73
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of (4-cyanophenyl)nitromethane (in water)
waterN  Parameter: 13.23
sN Parameter: 0.52
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of (4-nitrophenyl)nitromethane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 14.05
sN Parameter: 0.72
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of (4-nitrophenyl)nitromethane (in DMSO)
DMSON  Parameter: 16.29
sN Parameter: 0.75
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of (4-nitrophenyl)nitromethane (in water)
waterN  Parameter: 13.58
sN Parameter: 0.52
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of (4-NO2-C6H4)CH2SO2Ph (in DMSO)
DMSON  Parameter: 18.50
sN Parameter: 0.75
***Org. Biomol. Chem. 2008, 6, 3052-3058
DOI: 10.1039/b805604h
image of molecule

anion of (4-NO2-C6H4)CH2SO2Ph (in MeCN)
MeCNN  Parameter: 19.90
sN Parameter: 0.66
***J. Am. Chem. Soc. 2020, 142, 8383-8402
DOI: 10.1021/jacs.0c01960
image of molecule

anion of (benzylsulfonyl)benzene (in DMSO)
DMSON  Parameter: 25.77
sN Parameter: 0.56
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of (phenylmethylenedisulfonyl)dibenzene (in DMSO)
DMSON  Parameter: 15.07
sN Parameter: 0.79
***Eur. J. Org. Chem. 2017, , 1196-1202
DOI: 10.1002/ejoc.201601513
image of molecule

anion of 1,2,3-triphenylpropane-1,3-dione (in DMSO)
DMSON  Parameter: 14.99
sN Parameter: 0.83
***Eur. J. Org. Chem. 2017, , 1196-1202
DOI: 10.1002/ejoc.201601513
image of molecule

anion of 1,2-diphenylethanone (in DMSO)
DMSON  Parameter: 23.15
sN Parameter: 0.60
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of 1,3-diphenylpropane-1,3-dione (in DMSO)
DMSON  Parameter: 17.46
sN Parameter: 0.65
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of 1-phenyl-2-(phenylsulfonyl)ethanone (in DMSO)
DMSON  Parameter: 17.19
sN Parameter: 0.56
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of 1-phenylbutane-1,3-dione (in DMSO)
DMSON  Parameter: 16.03
sN Parameter: 0.86
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of 1-phenylpropan-2-one (in DMSO)
DMSON  Parameter: 24.99
sN Parameter: 0.60
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of 2-(4-CN-C6H4)propionitrile (in DMSO)
DMSON  Parameter: 25.35
sN Parameter: 0.56
***J. Org. Chem. 2009, 74, 75-81
DOI: 10.1021/jo802241x
image of molecule

anion of 2-(4-NO2-C6H4)propionitrile (in DMSO)
DMSON  Parameter: 19.61
sN Parameter: 0.60
***J. Org. Chem. 2009, 74, 75-81
DOI: 10.1021/jo802241x
image of molecule

anion of 2-nitro-1-phenylethan-1-one (in DMSO)
DMSON  Parameter: 13.91
sN Parameter: 0.76
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of 2-nitropropane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 12.20
sN Parameter: 0.71
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of 2-nitropropane (in DMSO)
DMSON  Parameter: 20.61
sN Parameter: 0.69
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of 2-nitropropane (in water)
waterN  Parameter: 10.69
sN Parameter: 0.56
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of 2-phenyl-2-(phenylsulfonyl)acetonitrile (in DMSO)
DMSON  Parameter: 15.97
sN Parameter: 0.72
***Eur. J. Org. Chem. 2017, , 1196-1202
DOI: 10.1002/ejoc.201601513
image of molecule

anion of 2-phenyl-propionitrile (in DMSO)
DMSON  Parameter: 28.95
sN Parameter: 0.58
***J. Org. Chem. 2009, 74, 75-81
DOI: 10.1021/jo802241x
image of molecule

anion of 2-phenylmalononitrile (in DMSO)
DMSON  Parameter: 15.58
sN Parameter: 1.00
***Eur. J. Org. Chem. 2017, , 1196-1202
DOI: 10.1002/ejoc.201601513
image of molecule

anion of 3-methyl acetylacetone (in DMSO)
DMSON  Parameter: 18.38
sN Parameter: 0.72
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of 3-methyl acetylacetone (in water)
waterN  Parameter: 14.33
sN Parameter: 0.69
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of 3-oxo-3-phenylpropanenitrile (in DMSO)
DMSON  Parameter: 16.55
sN Parameter: 0.78
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of 4-(trifluoromethyl)benzyl trifluoromethyl sulfone (in 91M9AN)
MeOH-MeCN mixN  Parameter: 20.72
sN Parameter: 0.58
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of 4-(trifluoromethyl)benzyl trifluoromethyl sulfone (in DMSO)
DMSON  Parameter: 17.33
sN Parameter: 0.74
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of 4-(trifluoromethyl)benzyl trifluoromethyl sulfone (in MeCN)
MeCNN  Parameter: 16.15
sN Parameter: 0.99
***J. Am. Chem. Soc. 2020, 142, 8383-8402
DOI: 10.1021/jacs.0c01960
image of molecule

anion of 4-(trifluoromethyl)benzyl-CN (in DMSO)
DMSON  Parameter: 27.28
sN Parameter: 0.50
***J. Org. Chem. 2009, 74, 75-81
DOI: 10.1021/jo802241x
image of molecule

anion of 4-cyanobenzyl trifluoromethyl sulfone (in 91M9AN)
MeOH-MeCN mixN  Parameter: 19.49
sN Parameter: 0.63
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of 4-cyanobenzyl trifluoromethyl sulfone (in DMSO)
DMSON  Parameter: 16.28
sN Parameter: 0.75
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of 4-cyanobenzyl trifluoromethyl sulfone (in MeCN)
MeCNN  Parameter: 15.62
sN Parameter: 0.99
***J. Am. Chem. Soc. 2020, 142, 8383-8402
DOI: 10.1021/jacs.0c01960
image of molecule

anion of 4-cyanobenzyl-CN (in DMSO)
DMSON  Parameter: 25.11
sN Parameter: 0.54
***J. Org. Chem. 2009, 74, 75-81
DOI: 10.1021/jo802241x
image of molecule

anion of 4-methylbenzyl trifluoromethyl sulfone (in DMSO)
DMSON  Parameter: 19.35
sN Parameter: 0.67
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of 4-nitrobenzyl trifluoromethyl sulfone (in 91M9AN)
MeOH-MeCN mixN  Parameter: 18.24
sN Parameter: 0.66
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of 4-nitrobenzyl trifluoromethyl sulfone (in DMSO)
DMSON  Parameter: 14.49
sN Parameter: 0.86
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of 4-nitrobenzyl-CN (in DMSO)
DMSON  Parameter: 19.67
sN Parameter: 0.68
***J. Org. Chem. 2009, 74, 75-81
DOI: 10.1021/jo802241x
image of molecule

anion of 4-nitrobenzyl-CN (in MeCN)
MeCNN  Parameter: 20.10
sN Parameter: 0.71
***J. Am. Chem. Soc. 2020, 142, 8383-8402
DOI: 10.1021/jacs.0c01960
image of molecule

anion of 5-(p-anisyl) Meldrum's acid (in DMSO)
DMSON  Parameter: 12.35
sN Parameter: 0.90
**Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of 5-phenyl Meldrum's acid (in DMSO)
DMSON  Parameter: 11.54
sN Parameter: 0.95
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of acetylacetone (in DMSO)
DMSON  Parameter: 17.64
sN Parameter: 0.73
***Angew. Chem. Int. Ed. 2002, 41, 91-95
DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
image of molecule

anion of acetylacetone (in water)
waterN  Parameter: 13.73
sN Parameter: 0.64
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of benzyl trifluoromethyl sulfone (in DMSO)
DMSON  Parameter: 18.67
sN Parameter: 0.68
***J. Am. Chem. Soc. 2007, 129, 9753-9761
DOI: 10.1021/ja072135b
image of molecule

anion of diethyl 2-(4-nitrophenyl)malonate (in DMSO)
DMSON  Parameter: 14.94
sN Parameter: 0.96
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl 2-(acetyl)malonate (in DMSO)
DMSON  Parameter: 13.83
sN Parameter: 0.84
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl 2-(benzoyl)malonate (in DMSO)
DMSON  Parameter: 13.63
sN Parameter: 0.80
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl 2-(isopropyl)malonate (in DMSO)
DMSON  Parameter: 18.74
sN Parameter: 0.71
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl 2-(p-anisyl)malonate (in DMSO)
DMSON  Parameter: 16.73
sN Parameter: 0.91
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl 2-butylmalonate (in DMSO)
DMSON  Parameter: 23.00
sN Parameter: 0.55
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl 2-cyclohexylmalonate (in DMSO)
DMSON  Parameter: 19.23
sN Parameter: 0.67
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl 2-phenylmalonate (in DMSO)
DMSON  Parameter: 15.93
sN Parameter: 0.99
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anion of diethyl malonate (in DMSO)
DMSON  Parameter: 20.22
sN Parameter: 0.65
***Angew. Chem. Int. Ed. 2002, 41, 91-95
DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
image of molecule

anion of diethyl malonate (in water)
waterN  Parameter: 16.15
sN Parameter: 0.66
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of diethyl methylmalonate (in DMSO)
DMSON  Parameter: 21.13
sN Parameter: 0.68
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of diethyl methylmalonate (in water)
waterN  Parameter: 17.68
sN Parameter: 0.50
*J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of dimedone (in DMSO)
DMSON  Parameter: 16.27
sN Parameter: 0.77
***Angew. Chem. Int. Ed. 2002, 41, 91-95
DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
image of molecule

anion of dimedone (in water)
waterN  Parameter: 11.77
sN Parameter: 0.63
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of dimethyl malonate (in 91M9AN)
MeOH-MeCN mixN  Parameter: 18.24
sN Parameter: 0.64
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of ethyl 2-cyano-2-phenylacetate (in DMSO)
DMSON  Parameter: 15.85
sN Parameter: 1.04
***Eur. J. Org. Chem. 2017, , 1196-1202
DOI: 10.1002/ejoc.201601513
image of molecule

anion of ethyl 2-nitroacetate (in DMSO)
DMSON  Parameter: 15.24
sN Parameter: 0.74
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of ethyl 3-oxo-3-phenylpropanoate (in DMSO)
DMSON  Parameter: 17.52
sN Parameter: 0.74
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of ethyl acetylacetate (in DMSO)
DMSON  Parameter: 18.82
sN Parameter: 0.69
***Angew. Chem. Int. Ed. 2002, 41, 91-95
DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
image of molecule

anion of ethyl acetylacetate (in water)
waterN  Parameter: 15.99
sN Parameter: 0.62
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of ethyl cyanoacetate (in 91M9AN)
MeOH-MeCN mixN  Parameter: 18.59
sN Parameter: 0.65
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of ethyl cyanoacetate (in DMSO)
DMSON  Parameter: 19.62
sN Parameter: 0.67
***Angew. Chem. Int. Ed. 2002, 41, 91-95
DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
image of molecule

anion of ethyl cyanoacetate (in water)
waterN  Parameter: 15.57
sN Parameter: 0.58
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of malononitrile (in 91M9AN)
MeOH-MeCN mixN  Parameter: 18.21
sN Parameter: 0.69
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of malononitrile (in DMSO)
DMSON  Parameter: 19.36
sN Parameter: 0.67
***Angew. Chem. Int. Ed. 2002, 41, 91-95
DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
image of molecule

anion of malononitrile (in water)
waterN  Parameter: 19.50
sN Parameter: 0.55
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of Meldrum's acid (in water)
waterN  Parameter: 12.06
sN Parameter: 0.66
***J. Am. Chem. Soc. 2003, 125, 12980-12986
DOI: 10.1021/ja036838e
image of molecule

anion of Meldrums acid (in DMSO)
DMSON  Parameter: 13.91
sN Parameter: 0.86
***Angew. Chem. Int. Ed. 2002, 41, 91-95
DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
image of molecule

anion of N,N-diethyl-3-oxo-3-phenylpropanoate (in DMSO)
DMSON  Parameter: 19.28
sN Parameter: 0.65
***Chem. Eur. J. 2015, 21, 875-884
DOI: 10.1002/chem.201404500
image of molecule

anion of nitroethane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.41
sN Parameter: 0.67
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of nitroethane (in DMF)
DMFN  Parameter: 22.21
sN Parameter: 0.48
***Chem. Eur. J. 2008, 14, 6108-6118
DOI: 10.1002/chem.200800329
image of molecule

anion of nitroethane (in DMSO)
DMSON  Parameter: 21.54
sN Parameter: 0.62
***J. Org. Chem. 2003, 68, 6880-6886
DOI: 10.1021/jo0344182
image of molecule

anion of nitroethane (in water)
waterN  Parameter: 11.25
sN Parameter: 0.52
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of nitromethane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 14.02
sN Parameter: 0.61
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of nitromethane (in DMSO)
DMSON  Parameter: 20.71
sN Parameter: 0.60
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of nitromethane (in water)
waterN  Parameter: 12.06
sN Parameter: 0.53
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of p-tolylnitromethane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.58
sN Parameter: 0.64
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of p-tolylnitromethane (in DMSO)
DMSON  Parameter: 18.31
sN Parameter: 0.76
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of p-tolylnitromethane (in water)
waterN  Parameter: 13.09
sN Parameter: 0.50
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of phenylnitromethane (in 91M9AN)
MeOH-MeCN mixN  Parameter: 12.51
sN Parameter: 0.67
***Eur. J. Org. Chem. 2006, , 2530-2537
DOI: 10.1002/ejoc.200500769
image of molecule

anion of phenylnitromethane (in DMSO)
DMSON  Parameter: 18.29
sN Parameter: 0.71
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of phenylnitromethane (in H2O)
waterN  Parameter: 12.05
sN Parameter: 0.53
***J. Org. Chem. 2004, 69, 7565-7576
DOI: 10.1021/jo048773j
image of molecule

anion of triethyl methanetricarboxylate (in DMSO)
DMSON  Parameter: 15.33
sN Parameter: 0.72
***Eur. J. Org. Chem. 2016, , 1841-1848
DOI: 10.1002/ejoc.201600107
image of molecule

anisole
dichloromethaneN  Parameter: -1.18
sN Parameter: 1.20
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

arginine (betaine, in water)
waterN  Parameter: 12.96
sN Parameter: 0.57
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

asparagine (anionic, in water)
waterN  Parameter: 13.03
sN Parameter: 0.53
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

aspartate (dianionic, in water)
waterN  Parameter: 13.81
sN Parameter: 0.53
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

azide ion (in 45M55AN)
MeOH-MeCN mixN  Parameter: 15.01
sN Parameter: 0.80
***J. Phys. Org. Chem. 2006, 19, 706-713
DOI: 10.1002/poc.1063
image of molecule

azide ion (in 91E9AN)
EtOH-MeCN mixN  Parameter: 16.30
sN Parameter: 0.73
***J. Phys. Org. Chem. 2006, 19, 706-713
DOI: 10.1002/poc.1063
image of molecule

azide ion (in 91iPr9AN)
iPrOH-MeCN mixN  Parameter: 17.07
sN Parameter: 0.71
***J. Phys. Org. Chem. 2006, 19, 706-713
DOI: 10.1002/poc.1063
image of molecule

azide ion (in 91M9AN)
MeOH-MeCN mixN  Parameter: 14.54
sN Parameter: 0.82
***J. Phys. Org. Chem. 2006, 19, 706-713
DOI: 10.1002/poc.1063
image of molecule

azide ion (in 91nPr9AN)
nPrOH-MeCN mixN  Parameter: 16.70
sN Parameter: 0.73
***J. Phys. Org. Chem. 2006, 19, 706-713
DOI: 10.1002/poc.1063
image of molecule

azide ion (in DMSO)
DMSON  Parameter: 20.50
sN Parameter: 0.59
***J. Phys. Org. Chem. 2006, 19, 706-713
DOI: 10.1002/poc.1063
image of molecule

azulene
MeCNN  Parameter: 6.66
sN Parameter: 1.02
***Eur. J. Org. Chem. 2009, , 1202-1206
DOI: 10.1002/ejoc.200801099
image of molecule

barbiturate anion (in DMSO)
DMSON  Parameter: 15.59
sN Parameter: 0.80
***J. Org. Chem. 2017, 82, 8476-8488
DOI: 10.1021/acs.joc.7b01223
image of molecule

benzimidazole (in DMSO)
DMSON  Parameter: 10.50
sN Parameter: 0.79
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

benzimidazole anion (in DMSO)
DMSON  Parameter: 19.13
sN Parameter: 0.55
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

benzoate (in 90AN10W)
aq MeCNN  Parameter: 11.30
sN Parameter: 0.72
**J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

benzoate (in MeCN)
MeCNN  Parameter: 16.82
sN Parameter: 0.70
***J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

benzoate (inMeCN)
MeCNN  Parameter: 16.45
sN Parameter: 0.72
***J. Am. Chem. Soc. 2020, 142, 5221-5233
DOI: 10.1021/jacs.9b12998
image of molecule

benzohydrazide (in MeCN)
MeCNN  Parameter: 12.49
sN Parameter: 0.66
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

benzotriazole (in MeCN)
MeCNN  Parameter: 7.69
sN Parameter: 0.76
*Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

benzotriazole anion (in DMSO)
DMSON  Parameter: 16.29
sN Parameter: 0.65
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

benzotriazole anion (in water)
waterN  Parameter: 11.52
sN Parameter: 0.67
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

benzyl (1-phenylvinyl)carbamate
MeCNN  Parameter: 6.21
sN Parameter: 0.87
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

benzyl isocyanide
dichloromethaneN  Parameter: 4.90
sN Parameter: 0.74
***Angew. Chem. Int. Ed. 2007, 46, 3563-3566
DOI: 10.1002/anie.200605205
image of molecule

benzylamine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.46
sN Parameter: 0.62
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

benzylamine (in DMSO)
DMSON  Parameter: 15.28
sN Parameter: 0.65
***J. Am. Chem. Soc. 2009, 131, 11392-11401
DOI: 10.1021/ja903207b
image of molecule

benzylamine (in MeCN)
MeCNN  Parameter: 14.29
sN Parameter: 0.67
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

benzylamine (in water)
waterN  Parameter: 13.44
sN Parameter: 0.55
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

benzyldimethylsilane
dichloromethaneN  Parameter: 2.78
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

beta-(trimethylsilyl)styrene
dichloromethaneN  Parameter: -0.43
sN Parameter: 1.06
***Chem. Eur. J. 2014, 20, 1103-1110
DOI: 10.1002/chem.201303215
image of molecule

beta-alanine (anionic, in water)
waterN  Parameter: 13.26
sN Parameter: 0.58
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

beta-piperidinium-peroxypropionate
waterN  Parameter: 13.94
sN Parameter: 0.62
***Eur. J. Org. Chem. 2018, , 6010-6017
DOI: 10.1002/ejoc.201801158
image of molecule

bis(4-(dimethylamino)phenyl)phenylmethane (in MeCN)
MeCNN  Parameter: -4.20
sN Parameter: 0.82
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

bis(4-methoxyphenyl)methane (in CH2Cl2)
dichloromethaneN  Parameter: -2.11
sN Parameter: 0.98
**J. Am. Chem. Soc. 2014, 136, 13863-13873
DOI: 10.1021/ja507598y
image of molecule

bis(4-methoxyphenyl)phenylmethane (in MeCN)
MeCNN  Parameter: -7.00
sN Parameter: 0.82
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

bis(4-nitrophenyl)methanide (in DMSO)
DMSON  Parameter: 19.92
sN Parameter: 0.67
***ARKIVOC 2008, (x), 37-53
DOI: 10.3998/ark.5550190.0009.a05
image of molecule

bis(phenylsulfonyl)methanide (in DMSO)
DMSON  Parameter: 15.68
sN Parameter: 0.74
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

borane-2,6-lutidine-complex
dichloromethaneN  Parameter: 10.33
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-4-methoxypyridine-complex
dichloromethaneN  Parameter: 11.01
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-4-tBu-pyridine-complex
dichloromethaneN  Parameter: 10.46
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-DMAP-complex
dichloromethaneN  Parameter: 12.44
sN Parameter: 0.76
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-N,N-diethylaniline-complex
dichloromethaneN  Parameter: 8.53
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-N,N-diisopropylaniline-complex
dichloromethaneN  Parameter: 8.84
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-N-ethyl-N-isopropylaniline-complex
dichloromethaneN  Parameter: 9.12
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-pyridine-complex
dichloromethaneN  Parameter: 10.01
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

borane-triethylamine-complex
dichloromethaneN  Parameter: 8.90
sN Parameter: 0.75
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

borane-trimethylamine-complex
dichloromethaneN  Parameter: 7.97
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

bromide (in 20% aq MeCN)
water-MeCN mixN  Parameter: 12.20
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

bromide (in 40% aq MeCN)
water-MeCN mixN  Parameter: 12.80
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

bromide (in 50% aq EtOH)
water-EtOH mixN  Parameter: 13.60
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

bromide (in 50% aq MeCN)
water-MeCN mixN  Parameter: 13.80
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

bromide (in 80% aq EtOH)
water-EtOH mixN  Parameter: 14.50
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

bromide (in CF3CH2OH)
TFEN  Parameter: 11.70
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

bromide (in H2O)
waterN  Parameter: 11.70
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

bromite (in water)
waterN  Parameter: 12.75
sN Parameter: 0.59
***Org. Lett. 2018, 20, 2816-2820
DOI: 10.1021/acs.orglett.8b00645
image of molecule

bromo(phenylsulfonyl)methanide (in DMSO)
DMSON  Parameter: 23.90
sN Parameter: 0.62
***J. Org. Chem. 2017, 82, 2011-2017
DOI: 10.1021/acs.joc.6b02844
image of molecule

bromoborane-triethylamine-complex
dichloromethaneN  Parameter: 7.49
sN Parameter: 0.75
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

Bu4NBH4 (in DMSO)
DMSON  Parameter: 14.94
sN Parameter: 0.79
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

buta-1,3-diene
dichloromethaneN  Parameter: -0.87
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

butyltrimethylsilane
dichloromethaneN  Parameter: -5.40
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

chloride (in 20% aq MeCN)
water-MeCN mixN  Parameter: 11.31
sN Parameter: 0.58
***J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in 40% aq MeCN)
water-MeCN mixN  Parameter: 11.30
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in 50% aq EtOH)
water-EtOH mixN  Parameter: 11.80
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in 50% aq MeCN)
water-MeCN mixN  Parameter: 12.00
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in 50/50 MeOH/MeCN)
MeOH-MeCN mixN  Parameter: 14.10
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in 60% aq MeCN)
water-MeCN mixN  Parameter: 12.00
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in 80% aq EtOH)
water-EtOH mixN  Parameter: 13.00
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in 80% aq MeCN)
water-MeCN mixN  Parameter: 13.30
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in CF3CH2OH)
TFEN  Parameter: 10.30
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in EtOH)
EtOHN  Parameter: 14.70
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in H2O)
waterN  Parameter: 10.10
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in hexafluoroisopropanol)
HFIPN  Parameter: 8.00
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in MeCN)
MeCNN  Parameter: 17.20
sN Parameter: 0.60
**J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloride (in MeOH)
MeOHN  Parameter: 12.90
sN Parameter: 0.60
*J. Am. Chem. Soc. 2005, 127, 2641-2649
DOI: 10.1021/ja045562n
image of molecule

chloro((4-chlorophenyl)sulfonyl)methanide (in DMSO)
DMSON  Parameter: 26.90
sN Parameter: 0.45
***J. Org. Chem. 2017, 82, 2011-2017
DOI: 10.1021/acs.joc.6b02844
image of molecule

chloro((4-cyanophenyl)sulfonyl)methanide (in DMSO)
DMSON  Parameter: 25.59
sN Parameter: 0.51
***J. Org. Chem. 2017, 82, 2011-2017
DOI: 10.1021/acs.joc.6b02844
image of molecule

chloro((4-nitrophenyl)sulfonyl)methanide (in DMSO)
DMSON  Parameter: 24.88
sN Parameter: 0.49
***J. Org. Chem. 2017, 82, 2011-2017
DOI: 10.1021/acs.joc.6b02844
image of molecule

chloro(phenylsulfonyl)methanide (in DMF)
DMFN  Parameter: 26.64
sN Parameter: 0.64
-Chem. Eur. J. 2008, 14, 6108-6118
DOI: 10.1002/chem.200800329
image of molecule

chloro(phenylsulfonyl)methanide (in DMSO)
DMSON  Parameter: 28.27
sN Parameter: 0.42
***J. Org. Chem. 2017, 82, 2011-2017
DOI: 10.1021/acs.joc.6b02844
image of molecule

chlorodimethylsilane
dichloromethaneN  Parameter: 0.79
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

cis-HMn(PCy3)(CO)4
dichloromethaneN  Parameter: 2.20
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

cis-HMn(PPh3)(CO)4
dichloromethaneN  Parameter: 2.30
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

cis-HRe(PPh3)(CO)4
dichloromethaneN  Parameter: 4.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

Cp2Ti(CH2Ph)2 - Dibenzyltitanocene
dichloromethaneN  Parameter: 4.38
sN Parameter: 1.00
*Chem. Eur. J. 2016, 22, 11196-11200
DOI: 10.1002/chem.201602452
image of molecule

Cp2Zr(CH2Ph)2 - Dibenzylzirconocene
dichloromethaneN  Parameter: 5.10
sN Parameter: 1.03
***Chem. Eur. J. 2016, 22, 11196-11200
DOI: 10.1002/chem.201602452
image of molecule

Cp2Zr(Me)2 - Dimethylzirconocene
dichloromethaneN  Parameter: 4.35
sN Parameter: 1.09
***Chem. Eur. J. 2016, 22, 11196-11200
DOI: 10.1002/chem.201602452
image of molecule

cumene peroxy anion (in H2O)
waterN  Parameter: 13.92
sN Parameter: 0.61
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

cyanamide anion (in DMSO)
DMSON  Parameter: 20.33
sN Parameter: 0.64
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

cyanate (in MeCN)
MeCNN  Parameter: 13.60
sN Parameter: 0.84
***Chem. Eur. J. 2008, 14, 3866-3868
DOI: 10.1002/chem.200800314
image of molecule

cyanide (in MeCN)
MeCNN  Parameter: 16.27
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2005, 44, 142-145
DOI: 10.1002/anie.200461640
image of molecule

cyano((diphenylmethylene)amino)methanide
DMSON  Parameter: 29.50
sN Parameter: 0.50
*Tetrahedron 2019, 75, 459-463
DOI: 10.1016/j.tet.2018.11.075
image of molecule

cyano(pyridin-1-ium-1-yl)methanide (in DMSO)
DMSON  Parameter: 25.94
sN Parameter: 0.42
***J. Am. Chem. Soc. 2013, 135, 15216-15224
DOI: 10.1021/ja407885h
image of molecule

cyanoborate ion (in water)
waterN  Parameter: 9.99
sN Parameter: 0.54
***Org. Biomol. Chem. 2023, 21, 85-88
DOI: 10.1039/D2OB02041F
image of molecule

cyclohepta-1,3,5-trienyl-Fe(CO)3
dichloromethaneN  Parameter: 3.42
sN Parameter: 0.94
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

cyclohepta-1,3-diene
dichloromethaneN  Parameter: 0.06
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

cycloheptatriene
dichloromethaneN  Parameter: 0.52
sN Parameter: 0.97
*J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

cycloheptatriene (in MeCN)
MeCNN  Parameter: 0.55
sN Parameter: 0.97
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

cyclohexa-1,3-diene
dichloromethaneN  Parameter: 0.67
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

cycloocta-1,3-diene
dichloromethaneN  Parameter: -0.50
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

cyclopentadiene
dichloromethaneN  Parameter: 2.30
sN Parameter: 1.06
***Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

cyclopentene
dichloromethaneN  Parameter: -1.55
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

cysteine (dianionic, in water, S-nucleophile!)
waterN  Parameter: 23.43
sN Parameter: 0.42
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

DABCO (in MeCN)
MeCNN  Parameter: 18.80
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2007, 46, 6176-6179
DOI: 10.1002/anie.200701489
image of molecule

Danishefskys diene
dichloromethaneN  Parameter: 8.57
sN Parameter: 0.84
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

DBN (in CH2Cl2)
dichloromethaneN  Parameter: 15.50
sN Parameter: 0.76
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

DBN (in MeCN)
MeCNN  Parameter: 16.28
sN Parameter: 0.67
***Chem. Commun. 2008, , 1792-1794
DOI: 10.1039/b801811a
image of molecule

DBU (in MeCN)
MeCNN  Parameter: 15.29
sN Parameter: 0.70
***Chem. Commun. 2008, , 1792-1794
DOI: 10.1039/b801811a
image of molecule

DBU (in THF)
THFN  Parameter: 16.12
sN Parameter: 0.67
***Angew. Chem. Int. Ed. 2011, 50, 6915-6919
DOI: 10.1002/anie.201102435
image of molecule

Desoxy Breslow intermediate 2a
THFN  Parameter: 17.12
sN Parameter: 0.80
***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
DOI: 10.1002/anie.201202327
image of molecule

Desoxy Breslow intermediate 2a
DMSON  Parameter: 17.41
sN Parameter: 0.74
***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
DOI: 10.1002/anie.201202327
image of molecule

Desoxy Breslow intermediate 2a'
THFN  Parameter: 14.45
sN Parameter: 0.71
***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
DOI: 10.1002/anie.201202327
image of molecule

Desoxy Breslow intermediate 2b
THFN  Parameter: 13.91
sN Parameter: 0.64
***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
DOI: 10.1002/anie.201202327
image of molecule

Desoxy Breslow intermediate 2b'
THFN  Parameter: 11.42
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
DOI: 10.1002/anie.201202327
image of molecule

Desoxy Breslow intermediate 2c'
THFN  Parameter: 12.75
sN Parameter: 0.71
***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
DOI: 10.1002/anie.201202327
image of molecule

Dexoxy Breslow intermediate 6
THFN  Parameter: 15.58
sN Parameter: 0.57
***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
DOI: 10.1002/anie.201204524
image of molecule

DHPB (3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine)
dichloromethaneN  Parameter: 13.86
sN Parameter: 0.78
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

di(methoxyethyl)amine (in MeCN)
MeCNN  Parameter: 13.24
sN Parameter: 0.93
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

diacetamide anion (in DMSO)
DMSON  Parameter: 16.05
sN Parameter: 0.70
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

diazoacetone
dichloromethaneN  Parameter: 3.96
sN Parameter: 0.91
***Chem. Eur. J. 2003, 9, 4068-4076
DOI: 10.1002/chem.200304913
image of molecule

diazocyclopentadiene (in CH2Cl2)
dichloromethaneN  Parameter: 4.84
sN Parameter: 1.06
***Synthesis 2023, 55, 354-358
DOI: 10.1055/s-0041-1737327
image of molecule

diazomethane
dichloromethaneN  Parameter: 10.48
sN Parameter: 0.78
***Chem. Eur. J. 2003, 9, 4068-4076
DOI: 10.1002/chem.200304913
image of molecule

dibutylsulfide (in CH2Cl2)
dichloromethaneN  Parameter: 11.86
sN Parameter: 0.74
**Chem. Eur. J. 2021, 21, 11367-11376
DOI: 10.1002/chem.202100977
image of molecule

dichloro(methyl)silane
dichloromethaneN  Parameter: -3.20
sN Parameter: 0.73
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

diethanolamine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.71
sN Parameter: 0.67
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

diethanolamine (in DMSO)
DMSON  Parameter: 15.51
sN Parameter: 0.70
***J. Am. Chem. Soc. 2009, 131, 11392-11401
DOI: 10.1021/ja903207b
image of molecule

diethanolamine (in water)
waterN  Parameter: 13.00
sN Parameter: 0.61
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

diethyl diazomalonate
dichloromethaneN  Parameter: -0.35
sN Parameter: 0.93
**Chem. Eur. J. 2003, 9, 4068-4076
DOI: 10.1002/chem.200304913
image of molecule

diethyl(methyl)silane
dichloromethaneN  Parameter: 3.40
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

diethylamine (in MeCN)
MeCNN  Parameter: 15.10
sN Parameter: 0.73
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

diethylamine (in water)
waterN  Parameter: 14.68
sN Parameter: 0.53
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

diethylether (in dichloromethane)
dichloromethaneN  Parameter: -5.10
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

diethylmercury (in MeCN)
MeCNN  Parameter: -0.70
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dihexylsilane
dichloromethaneN  Parameter: 2.27
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

Dimedone iodonium ylide (in CH2Cl2)
dichloromethaneN  Parameter: 6.18
sN Parameter: 0.81
***J. Am. Chem. Soc. 2016, 138, 10304-10313
DOI: 10.1021/jacs.6b05768
image of molecule

dimethoxymethane
dichloromethaneN  Parameter: -4.90
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

Dimethyl 1,1'-isopropylidenezirconocene
dichloromethaneN  Parameter: 5.20
sN Parameter: 1.00
*Chem. Eur. J. 2016, 22, 11196-11200
DOI: 10.1002/chem.201602452
image of molecule

Dimethyl bis(indenyl)zirconium(IV)
dichloromethaneN  Parameter: 6.89
sN Parameter: 1.00
*Chem. Eur. J. 2016, 22, 11196-11200
DOI: 10.1002/chem.201602452
image of molecule

dimethyl diazomalonate
dichloromethaneN  Parameter: -1.24
sN Parameter: 0.81
***Angew. Chem. Int. Ed. Engl. 1994, 33, 938-957
DOI: 10.1002/anie.199409381
image of molecule

dimethyl((trimethylgermyl)methyl)silane
dichloromethaneN  Parameter: 5.36
sN Parameter: 0.62
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dimethyl((trimethylstannyl)methyl)silane
dichloromethaneN  Parameter: 6.53
sN Parameter: 0.58
**Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dimethyl(neopentyl)silane
dichloromethaneN  Parameter: 3.55
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dimethyl(p-tolyl)silane
dichloromethaneN  Parameter: 3.83
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dimethyl(phenyl)silane
dichloromethaneN  Parameter: 3.55
sN Parameter: 0.75
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dimethyl(propoxy)silane
dichloromethaneN  Parameter: 2.40
sN Parameter: 0.75
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dimethylamine (in MeCN)
MeCNN  Parameter: 17.96
sN Parameter: 0.63
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

dimethylamine (in water)
waterN  Parameter: 17.12
sN Parameter: 0.50
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

dimethylselenide (in CH2Cl2)
dichloromethaneN  Parameter: 12.60
sN Parameter: 0.72
-Chem. Eur. J. 2021, 21, 11367-11376
DOI: 10.1002/chem.202100977
image of molecule

dimethylsulfide (in CH2Cl2)
dichloromethaneN  Parameter: 12.32
sN Parameter: 0.72
**Chem. Eur. J. 2021, 21, 11367-11376
DOI: 10.1002/chem.202100977
image of molecule

dimethylsulfide (in MeCN)
MeCNN  Parameter: 12.70
sN Parameter: 0.72
-Chem. Eur. J. 2021, 21, 11367-11376
DOI: 10.1002/chem.202100977
image of molecule

diphenyldiazomethane
dichloromethaneN  Parameter: 5.29
sN Parameter: 0.92
***Chem. Eur. J. 2003, 9, 4068-4076
DOI: 10.1002/chem.200304913
image of molecule

diphenylsilane
dichloromethaneN  Parameter: 1.52
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

dipp Imd boronate
dichloromethaneN  Parameter: 9.55
sN Parameter: 0.81
***Org. Lett. 2012, 14, 82-85
DOI: 10.1021/ol202836p
image of molecule

dipropylamine (in MeCN)
MeCNN  Parameter: 14.51
sN Parameter: 0.80
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

ditert-butyl-phenylphosphane
dichloromethaneN  Parameter: 12.40
sN Parameter: 0.55
-Chem. Eur. J. 2017, 23, 7422-7427
DOI: 10.1002/chem.201701080
image of molecule

DMSO (O attack)
DMSON  Parameter: 11.30
sN Parameter: 0.74
***J. Am. Chem. Soc. 2009, 131, 11392-11401
DOI: 10.1021/ja903207b
image of molecule

enolate of 2-coumaranone (in DMSO)
DMSON  Parameter: 19.60
sN Parameter: 0.75
***J. Org. Chem. 2024, 89, 6915-6928
DOI: 10.1021/acs.joc.4c00277
image of molecule

enolate of 3-isochromanone (in DMSO)
DMSON  Parameter: 25.39
sN Parameter: 0.54
***J. Org. Chem. 2024, 89, 6915-6928
DOI: 10.1021/acs.joc.4c00277
image of molecule

ethanol
EtOHN  Parameter: 7.44
sN Parameter: 0.90
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

ethanol (in MeCN)
MeCNN  Parameter: 7.13
sN Parameter: 0.71
***Bull. Chem. Soc. Jpn. 2018, 91, 523-530
DOI: 10.1246/bcsj.20170360
image of molecule

ethanolamine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.23
sN Parameter: 0.65
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

ethanolamine (in DMSO)
DMSON  Parameter: 16.07
sN Parameter: 0.61
***J. Am. Chem. Soc. 2009, 131, 11392-11401
DOI: 10.1021/ja903207b
image of molecule

ethanolamine (in MeCN)
MeCNN  Parameter: 14.11
sN Parameter: 0.71
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

ethanolamine (in water)
waterN  Parameter: 12.61
sN Parameter: 0.58
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

ethanolate (in 91E9AN)
EtOH-MeCN mixN  Parameter: 16.08
sN Parameter: 0.62
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

ethanolate (in ethanol)
EtOHN  Parameter: 15.78
sN Parameter: 0.65
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

ethyl (E)-3-(dimethylamino)acrylate
dichloromethaneN  Parameter: 9.43
sN Parameter: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

ethyl (E)-3-(N-morpholino)acrylate
dichloromethaneN  Parameter: 8.52
sN Parameter: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

ethyl diazoacetate
dichloromethaneN  Parameter: 4.91
sN Parameter: 0.95
***Chem. Eur. J. 2003, 9, 4068-4076
DOI: 10.1002/chem.200304913
image of molecule

ethyl glycinate (in DMSO)
DMSON  Parameter: 14.30
sN Parameter: 0.67
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

ethyl N-acetylcarbamate anion (in DMSO)
DMSON  Parameter: 15.99
sN Parameter: 0.70
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

ethyl-vinylether
dichloromethaneN  Parameter: 3.92
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

ethylamine (in water)
waterN  Parameter: 12.87
sN Parameter: 0.58
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

ethyldimethylsilane
dichloromethaneN  Parameter: 3.30
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

ethylenediamine (in water)
waterN  Parameter: 13.28
sN Parameter: 0.58
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

fluoride (in 10 % aq MeCN)
water-MeCN mixN  Parameter: 8.05
sN Parameter: 0.64
***J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluoride (in 60% aq MeCN)
water-MeCN mixN  Parameter: 9.75
sN Parameter: 0.63
***J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluoride (in 80% aq EtOH)
water-EtOH mixN  Parameter: 13.20
sN Parameter: 0.53
*J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluoride (in 80% aq MeCN)
water-MeCN mixN  Parameter: 11.40
sN Parameter: 0.59
***J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluoride (in 90% aq MeCN)
water-MeCN mixN  Parameter: 12.27
sN Parameter: 0.59
***J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluoride (in 98% aq MeCN)
water-MeCN mixN  Parameter: 10.88
sN Parameter: 0.83
***J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluoride (in MeOH)
MeOHN  Parameter: 11.31
sN Parameter: 0.63
***J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluoride (in water)
waterN  Parameter: 7.70
sN Parameter: 0.66
*J. Org. Chem. 2012, 77, 3325-3335
DOI: 10.1021/jo300141z
image of molecule

fluorobis(phenylsulfonyl)methanide (in DMSO)
DMSON  Parameter: 17.46
sN Parameter: 0.73
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

formohydrazide (in MeCN)
MeCNN  Parameter: 10.35
sN Parameter: 0.76
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

furan
dichloromethaneN  Parameter: 1.33
sN Parameter: 1.29
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

gamma-aminobutyric acid (anionic, in water)
waterN  Parameter: 13.55
sN Parameter: 0.56
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

glutamate (dianionic, in water)
waterN  Parameter: 13.96
sN Parameter: 0.54
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

glutamine (anionic, in water)
waterN  Parameter: 13.45
sN Parameter: 0.54
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

glutathione GSH(NH3+/S-)
waterN  Parameter: 20.97
sN Parameter: 0.56
***Angew. Chem. Int. Ed. 2019, 58, 17704-17708
DOI: 10.1002/anie.201909803
image of molecule

glycine (anionic, in water)
waterN  Parameter: 13.51
sN Parameter: 0.58
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

glycineamide (in water)
waterN  Parameter: 12.29
sN Parameter: 0.58
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

glycinenitrile (in water)
waterN  Parameter: 10.80
sN Parameter: 0.61
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

glycylglycine (anionic, in water)
waterN  Parameter: 12.91
sN Parameter: 0.59
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

glycylglycylglycine (anionic, in water)
waterN  Parameter: 12.26
sN Parameter: 0.63
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

guanine anion (in water)
waterN  Parameter: 11.63
sN Parameter: 0.59
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

guanosine anion (in water)
waterN  Parameter: 12.09
sN Parameter: 0.52
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

H2O (in water)
waterN  Parameter: 5.20
sN Parameter: 0.89
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

Hantzsch ester
dichloromethaneN  Parameter: 9.00
sN Parameter: 0.90
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

HCr(CO)3Cp*
dichloromethaneN  Parameter: 1.60
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

hexylsilane
dichloromethaneN  Parameter: 0.19
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HFe(CO)2Cp*
dichloromethaneN  Parameter: 8.20
sN Parameter: 0.69
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

histidine (anionic, in water)
waterN  Parameter: 13.83
sN Parameter: 0.54
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

HMn(CO)5
dichloromethaneN  Parameter: 1.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HMo(CO)3Cp*
dichloromethaneN  Parameter: 4.30
sN Parameter: 0.77
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HMo(Cp)(CO)3
dichloromethaneN  Parameter: 4.88
sN Parameter: 0.80
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HOO- (in water)
waterN  Parameter: 15.40
sN Parameter: 0.55
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

HOs(CO)2Cp*
dichloromethaneN  Parameter: 5.20
sN Parameter: 0.95
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HRe(CO)5
dichloromethaneN  Parameter: 3.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HRu(CO)2Cp*
dichloromethaneN  Parameter: 8.00
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HW(CO)3(C5H4CO2Me)
dichloromethaneN  Parameter: -0.90
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HW(CO)3(C5H4Me)
dichloromethaneN  Parameter: 2.40
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HW(CO)3(indenyl)
dichloromethaneN  Parameter: 3.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HW(CO)3Cp
dichloromethaneN  Parameter: 1.70
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HW(CO)3Cp*
dichloromethaneN  Parameter: 3.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

HW(NO)2Cp
dichloromethaneN  Parameter: 4.70
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

hydantoin anion (in DMSO)
DMSON  Parameter: 17.52
sN Parameter: 0.55
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

hydrazine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.47
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

hydrazine (in MeCN)
MeCNN  Parameter: 16.45
sN Parameter: 0.56
***Angew. Chem. Int. Ed. 2012, 51, 1353-1356
DOI: 10.1002/anie.201107315
image of molecule

hydrazine (in water)
waterN  Parameter: 13.46
sN Parameter: 0.57
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

hydroxylamine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 12.23
sN Parameter: 0.66
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

hydroxylamine (in MeCN)
MeCNN  Parameter: 12.80
sN Parameter: 0.63
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

hydroxylamine (in water)
waterN  Parameter: 11.41
sN Parameter: 0.55
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

hypobromite (in water)
waterN  Parameter: 16.69
sN Parameter: 0.46
***Org. Lett. 2018, 20, 2816-2820
DOI: 10.1021/acs.orglett.8b00645
image of molecule

hypochlorite (in water)
waterN  Parameter: 14.50
sN Parameter: 0.58
***Org. Lett. 2018, 20, 2816-2820
DOI: 10.1021/acs.orglett.8b00645
image of molecule

imidazole (in 91M9AN)
MeOH-MeCN mixN  Parameter: 10.41
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

imidazole (in DMSO)
DMSON  Parameter: 11.58
sN Parameter: 0.79
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

imidazole (in MeCN)
MeCNN  Parameter: 11.47
sN Parameter: 0.79
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

imidazole (in water)
waterN  Parameter: 9.63
sN Parameter: 0.57
***Org. Biomol. Chem. 2010, 8, 1929-1935
DOI: 10.1039/c000965b
image of molecule

imidazole anion (in DMSO)
DMSON  Parameter: 21.09
sN Parameter: 0.51
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

Indole
dichloromethaneN  Parameter: 5.55
sN Parameter: 1.09
***J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

isobutylenyl-ethylether
dichloromethaneN  Parameter: 4.23
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

isopropanol (in aq. sulfuric acid)
waterN  Parameter: -2.60
sN Parameter: 0.80
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

isopropanol (in MeCN)
MeCNN  Parameter: 6.82
sN Parameter: 0.70
***Bull. Chem. Soc. Jpn. 2018, 91, 523-530
DOI: 10.1246/bcsj.20170360
image of molecule

isopropanolate (in 91iPr9AN)
iPrOH-MeCN mixN  Parameter: 17.71
sN Parameter: 0.58
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

isopropanolate (in propan-2-ol)
iPrOHN  Parameter: 17.03
sN Parameter: 0.63
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

isopropylamine (in MeCN)
MeCNN  Parameter: 13.77
sN Parameter: 0.70
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

isopropylamine (in water)
waterN  Parameter: 12.00
sN Parameter: 0.56
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

KBH4 (in DMSO)
DMSON  Parameter: 15.14
sN Parameter: 0.77
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

leucine (anionic, in water)
waterN  Parameter: 14.01
sN Parameter: 0.52
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

lithium (5-methylfuran-2-yl)(4-(trifluoromethyl)phenyl)pinacolborate
MeCNN  Parameter: 8.13
sN Parameter: 0.85
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)glycolborate
MeCNN  Parameter: 11.23
sN Parameter: 0.77
***Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)neopentylglycolborate
MeCNN  Parameter: 10.13
sN Parameter: 0.91
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)pinacolborate
MeCNN  Parameter: 5.53
sN Parameter: 1.00
*Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(4-(dimethylamino)phenyl)pinacolborate
MeCNN  Parameter: 8.02
sN Parameter: 0.89
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)catecholglycolborate
MeCNN  Parameter: 6.50
sN Parameter: 0.77
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)neopentylglycolborate
MeCNN  Parameter: 11.85
sN Parameter: 0.72
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(4-chlorophenyl)pinacolborate
MeCNN  Parameter: 6.77
sN Parameter: 0.88
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(4-methoxyphenyl)pinacolborate
MeCNN  Parameter: 7.51
sN Parameter: 0.87
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(4-methylphenyl)pinacolborate
MeCNN  Parameter: 6.98
sN Parameter: 0.93
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (5-methylthiophen-2-yl)(phenyl)pinacolborate
MeCNN  Parameter: 7.24
sN Parameter: 0.83
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium (E)-2-(3,5-bis(trifluoromethyl)phenyl)-2-(but-2-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 9.49
sN Parameter: 0.82
***J. Am. Chem. Soc. 2017, 139, 15324-15327
DOI: 10.1021/jacs.7b10240
image of molecule

lithium 2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 7.46
sN Parameter: 0.76
**Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 2-allyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 8.71
sN Parameter: 0.80
***J. Am. Chem. Soc. 2017, 139, 15324-15327
DOI: 10.1021/jacs.7b10240
image of molecule

lithium 2-allyl-4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 11.20
sN Parameter: 0.64
*J. Am. Chem. Soc. 2017, 139, 15324-15327
DOI: 10.1021/jacs.7b10240
image of molecule

lithium 2-benzyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 6.30
sN Parameter: 0.78
**Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 2-benzyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 7.15
sN Parameter: 0.77
***Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 2-benzyl-4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 8.92
sN Parameter: 0.70
**Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 2-cyclopropyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 7.72
sN Parameter: 0.75
*Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 2-ethyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 7.68
sN Parameter: 0.78
***Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 2-isopropyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 6.63
sN Parameter: 0.75
*Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 4,4,5,5-tetramethyl-2-(1-phenylethyl)-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 8.56
sN Parameter: 0.76
***Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 4,4,5,5-tetramethyl-2-phenyl-2-(1-phenylethyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 10.97
sN Parameter: 0.63
**Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium 4,4,5,5-tetramethyl-2-phenyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolan-2-uide (in MeCN)
MeCNN  Parameter: 11.00
sN Parameter: 0.57
***J. Am. Chem. Soc. 2022, 144, 16118-16130
DOI: 10.1021/jacs.2c06493
image of molecule

lithium 5,5-dimethyl-2-(1-phenylethyl)-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborinan-2-uide (in MeCN)
MeCNN  Parameter: 11.29
sN Parameter: 0.76
***Org. Lett. 2015, 17, 2614-2617
DOI: 10.1021/acs.orglett.5b00918
image of molecule

lithium bis(5-methylthiophen-2-yl)pinacolborate
MeCNN  Parameter: 7.67
sN Parameter: 0.87
**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
DOI: 10.1002/anie.201410562
image of molecule

lithium indenide (in DMSO)
DMSON  Parameter: 23.66
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2015, 54, 12497-12500
DOI: 10.1002/anie.201501385
image of molecule

m-(trifluoromethyl)phenolate (in DMF)
DMFN  Parameter: 23.40
sN Parameter: 0.51
*J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

m-(trifluoromethyl)phenolate (in DMSO)
DMSON  Parameter: 22.62
sN Parameter: 0.51
**J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

m-(trifluoromethyl)phenolate (in MeCN)
MeCNN  Parameter: 23.20
sN Parameter: 0.51
*J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

m-methoxyphenolate (in MeCN)
MeCNN  Parameter: 18.81
sN Parameter: 0.80
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

m-nitrophenolate (in DMF)
DMFN  Parameter: 22.41
sN Parameter: 0.54
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

m-nitrophenolate (in DMSO)
DMSON  Parameter: 21.29
sN Parameter: 0.54
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

m-nitrophenolate (in MeCN)
MeCNN  Parameter: 25.51
sN Parameter: 0.43
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

m-xylene
dichloromethaneN  Parameter: -3.57
sN Parameter: 2.08
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

magnesium 2-carboperoxybenzoate (in H2O)
waterN  Parameter: 18.43
sN Parameter: 0.46
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

maleimide anion (in DMSO)
DMSON  Parameter: 14.87
sN Parameter: 0.76
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

Me2 Imd boronate
dichloromethaneN  Parameter: 11.88
sN Parameter: 0.71
***Org. Lett. 2012, 14, 82-85
DOI: 10.1021/ol202836p
image of molecule

Me2S(O)=CH2 (in DMSO)
DMSON  Parameter: 21.29
sN Parameter: 0.47
***J. Am. Chem. Soc. 2010, 132, 17894-17900
DOI: 10.1021/ja1084749
image of molecule

Me2S=CH(4-CN-C6H4) (in DMSO)
DMSON  Parameter: 21.07
sN Parameter: 0.68
***J. Am. Chem. Soc. 2010, 132, 17894-17900
DOI: 10.1021/ja1084749
image of molecule

Me2S=CH(p-NO2-C6H4) (in DMSO)
DMSON  Parameter: 18.42
sN Parameter: 0.65
***J. Am. Chem. Soc. 2010, 132, 17894-17900
DOI: 10.1021/ja1084749
image of molecule

Me2S=CH-CN (in DMSO)
DMSON  Parameter: 16.23
sN Parameter: 0.60
***Chem. Eur. J. 2010, 16, 8610-8614
DOI: 10.1002/chem.201001455
image of molecule

Me2S=CH-CO2Et (in DMSO)
DMSON  Parameter: 15.85
sN Parameter: 0.61
***Chem. Eur. J. 2010, 16, 8610-8614
DOI: 10.1002/chem.201001455
image of molecule

Meldrum's acid iodonium ylide (in CH2Cl2)
dichloromethaneN  Parameter: 4.36
sN Parameter: 1.06
***J. Am. Chem. Soc. 2016, 138, 10304-10313
DOI: 10.1021/jacs.6b05768
image of molecule

MeO-Breslow 1a
THFN  Parameter: 14.77
sN Parameter: 0.80
***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
DOI: 10.1002/anie.201204524
image of molecule

MeO-Breslow 1b
THFN  Parameter: 10.45
sN Parameter: 0.81
***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
DOI: 10.1002/anie.201204524
image of molecule

MeO-Breslow 1c
THFN  Parameter: 16.61
sN Parameter: 0.68
***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
DOI: 10.1002/anie.201204524
image of molecule

MeO-Breslow 1e
THFN  Parameter: 15.65
sN Parameter: 0.52
***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
DOI: 10.1002/anie.201204524
image of molecule

MeSO-CH-CO2Et (in DMSO)
DMSON  Parameter: 20.61
sN Parameter: 0.64
***Chem. Eur. J. 2010, 16, 8610-8614
DOI: 10.1002/chem.201001455
image of molecule

MeSO2-CH-CO2Et (in DMSO)
DMSON  Parameter: 18.00
sN Parameter: 0.66
***Chem. Eur. J. 2010, 16, 8610-8614
DOI: 10.1002/chem.201001455
image of molecule

methanesulfonamide anion (in DMSO)
DMSON  Parameter: 18.61
sN Parameter: 0.53
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

methanol
MeOHN  Parameter: 7.54
sN Parameter: 0.92
***J. Am. Chem. Soc. 2004, 126, 5174-5181
DOI: 10.1021/ja031828z
image of molecule

methanol (in MeCN)
MeCNN  Parameter: 6.86
sN Parameter: 0.73
***Bull. Chem. Soc. Jpn. 2018, 91, 523-530
DOI: 10.1246/bcsj.20170360
image of molecule

methanolate (in 91M9AN)
MeOH-MeCN mixN  Parameter: 14.51
sN Parameter: 0.68
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

methanolate (in methanol)
MeOHN  Parameter: 15.78
sN Parameter: 0.56
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

methionine (anionic, in water)
waterN  Parameter: 13.16
sN Parameter: 0.58
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

methoxybis(phenylsulfonyl)methanide (in DMSO)
DMSON  Parameter: 17.29
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
DOI: 10.1002/anie.201605616
image of molecule

methyl (cyclohexen-1-yl)prolinate (in MeCN)
MeCNN  Parameter: 14.96
sN Parameter: 0.68
***Angew. Chem. Int. Ed. 2010, 49, 9526-9529
DOI: 10.1002/anie.201004344
image of molecule

methyl carbonate (in MeCN)
MeCNN  Parameter: 16.03
sN Parameter: 0.64
***Eur. J. Org. Chem. 2010, , 4205-4210
DOI: 10.1002/ejoc.201000414
image of molecule

methyl diazoacetate
dichloromethaneN  Parameter: 4.68
sN Parameter: 0.94
***J. Am. Chem. Soc. 2023, 145, 7416-7434
DOI: 10.1021/jacs.2c13872
image of molecule

methyl glycinate (in water)
waterN  Parameter: 12.08
sN Parameter: 0.60
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

methyl L-prolinate
MeCNN  Parameter: 14.75
sN Parameter: 0.82
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

methyl(neopentyl)(phenyl)silane
dichloromethaneN  Parameter: 0.87
sN Parameter: 0.75
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

methyl(phenyl)silane
dichloromethaneN  Parameter: 2.13
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

methylamine (in MeCN)
MeCNN  Parameter: 15.19
sN Parameter: 0.68
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

methylamine (in water)
waterN  Parameter: 13.85
sN Parameter: 0.53
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

methyldiphenylsilane
dichloromethaneN  Parameter: 2.72
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

methylenecyclobutane
dichloromethaneN  Parameter: 1.65
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecyclodecane
dichloromethaneN  Parameter: 2.82
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecyclododecane
dichloromethaneN  Parameter: 1.52
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecycloheptane
dichloromethaneN  Parameter: 2.24
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecyclohexane
dichloromethaneN  Parameter: 1.16
sN Parameter: 1.04
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

methylenecyclononane
dichloromethaneN  Parameter: 2.57
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecyclooctane
dichloromethaneN  Parameter: 3.16
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecyclopentadecane
dichloromethaneN  Parameter: 1.69
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecyclopentane
dichloromethaneN  Parameter: 2.82
sN Parameter: 0.90
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

methylenecyclopropane
dichloromethaneN  Parameter: -0.47
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylenecycloundecane
dichloromethaneN  Parameter: 2.33
sN Parameter: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

methylhydrazine (in MeCN)
MeCNN  Parameter: 17.73
sN Parameter: 0.58
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

methylhydrazine (in water)
waterN  Parameter: 17.23
sN Parameter: 0.45
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

morpholin-1-yl dithiocarbamate (in MeCN)
MeCNN  Parameter: 21.72
sN Parameter: 0.64
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

morpholine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 15.40
sN Parameter: 0.64
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

morpholine (in DMSO)
DMSON  Parameter: 16.96
sN Parameter: 0.67
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

morpholine (in MeCN)
MeCNN  Parameter: 15.65
sN Parameter: 0.74
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

morpholine (in water)
waterN  Parameter: 15.62
sN Parameter: 0.54
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

morpholinoisobutylene
dichloromethaneN  Parameter: 10.04
sN Parameter: 0.82
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

N',N'-dimethylformohydrazide (in MeCN)
MeCNN  Parameter: 15.69
sN Parameter: 0.51
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

N,N-dimethyl dithiocarbamate (in MeCN)
MeCNN  Parameter: 20.93
sN Parameter: 0.69
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

N,N-Dimethylbarbituric acid iodonium ylide (in CHCl2)
dichloromethaneN  Parameter: 7.98
sN Parameter: 0.71
***J. Am. Chem. Soc. 2016, 138, 10304-10313
DOI: 10.1021/jacs.6b05768
image of molecule

N-(1,3-dimethylimidazolidin-2-ylidene)-1-phenylmethanamine
dichloromethaneN  Parameter: 14.00
sN Parameter: 0.70
***ChemCatChem 2012, 4, 993-999
DOI: 10.1002/cctc.201200143
image of molecule

N-(1-(4-chlorophenyl)vinyl)acetamide
MeCNN  Parameter: 5.60
sN Parameter: 1.00
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(1-(4-methoxyphenyl)vinyl)acetamide
MeCNN  Parameter: 7.06
sN Parameter: 0.85
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(1-(naphthalen-2-yl)vinyl)acetamide
MeCNN  Parameter: 6.28
sN Parameter: 0.95
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(1-(p-tolyl)vinyl)acetamide
MeCNN  Parameter: 6.57
sN Parameter: 0.91
**Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(1-phenylvinyl)acetamide
MeCNN  Parameter: 5.73
sN Parameter: 0.97
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(1-phenylvinyl)benzamide
MeCNN  Parameter: 5.44
sN Parameter: 1.00
*Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(3,3-dimethylbut-1-en-2-yl)acetamide
MeCNN  Parameter: 4.61
sN Parameter: 0.98
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(3,4-dihydronaphthalen-1-yl)acetamide
MeCNN  Parameter: 4.91
sN Parameter: 0.87
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(cyclohex-1-en-1-yl)acetamide
MeCNN  Parameter: 5.64
sN Parameter: 0.79
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(cyclopent-1-en-1-yl)acetamide
MeCNN  Parameter: 7.06
sN Parameter: 0.87
***Chem. Eur. J. 2012, 18, 5732-5740
DOI: 10.1002/chem.201103519
image of molecule

N-(p-anisyl)-1,4-dihydronicotineamide
dichloromethaneN  Parameter: 8.11
sN Parameter: 0.92
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

N-(p-tolyl)-1,4-dihydronicotineamide
dichloromethaneN  Parameter: 7.68
sN Parameter: 0.95
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

N-(phenylmethyl)propan-2-imine (in CH2Cl2)
dichloromethaneN  Parameter: 11.13
sN Parameter: 0.73
***Z. Naturforsch. B 2013, 68b, 693-699
DOI: 10.5560/ZNB.2013-3085
image of molecule

N-(triisopropylsilyl)pyrrole
dichloromethaneN  Parameter: 3.12
sN Parameter: 0.93
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

N-benzyl-1,4-dihydronicotineamide
dichloromethaneN  Parameter: 8.67
sN Parameter: 0.82
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

N-benzyl-1,4-dihydronicotineamide (in 50W50AN)
water-MeCN mixN  Parameter: 9.79
sN Parameter: 0.70
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

N-benzyl-1,4-dihydronicotineamide (in 67W33AN)
water-MeCN mixN  Parameter: 10.19
sN Parameter: 0.70
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

N-benzyl-1,4-dihydronicotineamide (in 80W20AN)
water-MeCN mixN  Parameter: 10.67
sN Parameter: 0.70
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

N-benzyl-1,4-dihydronicotineamide (in 90W10AN)
water-MeCN mixN  Parameter: 11.35
sN Parameter: 0.66
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

N-benzyl-1,4-dihydronicotineamide (in MeCN)
MeCNN  Parameter: 9.80
sN Parameter: 0.70
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

N-benzyl-N-((2-methoxyphenyl)ethynyl)-4-methylbenzenesulfonamide
dichloromethaneN  Parameter: 4.40
sN Parameter: 0.86
***Angew. Chem. Int. Ed. 2014, 53, 4968-4971
DOI: 10.1002/anie.201402055
image of molecule

N-benzyl-N-(but-1-yn-1-yl)-4-methylbenzenesulfonamide
dichloromethaneN  Parameter: 5.16
sN Parameter: 0.85
***Angew. Chem. Int. Ed. 2014, 53, 4968-4971
DOI: 10.1002/anie.201402055
image of molecule

n-butyl vinyl ether
dichloromethaneN  Parameter: 3.76
sN Parameter: 0.91
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

n-butylamine (in MeCN)
MeCNN  Parameter: 15.27
sN Parameter: 0.63
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

N-methyl-1-phenylmethanimine (in CH2Cl2)
dichloromethaneN  Parameter: 8.60
sN Parameter: 0.77
***Z. Naturforsch. B 2013, 68b, 693-699
DOI: 10.5560/ZNB.2013-3085
image of molecule

N-methyl-glycinenitrile (in water)
waterN  Parameter: 13.50
sN Parameter: 0.59
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

N-methyl-morpholine (in CH2Cl2)
dichloromethaneN  Parameter: 16.50
sN Parameter: 0.52
*J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

N-methyl-morpholine (in MeCN)
MeCNN  Parameter: 16.80
sN Parameter: 0.52
*J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

N-methyl-piperidine (in CH2Cl2)
dichloromethaneN  Parameter: 18.90
sN Parameter: 0.52
*J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

N-methyl-piperidine (in MeCN)
MeCNN  Parameter: 18.72
sN Parameter: 0.52
***J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

N-methyl-pyrrolidine (in CH2Cl2)
dichloromethaneN  Parameter: 20.60
sN Parameter: 0.52
*J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

N-methyl-pyrrolidine (in MeCN)
MeCNN  Parameter: 20.59
sN Parameter: 0.52
***J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

N-methyl-trifluoroacetamide anion (in DMSO)
DMSON  Parameter: 15.70
sN Parameter: 0.71
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

N-methylenepyrrolidin-1-amine (in CH2Cl2)
dichloromethaneN  Parameter: 7.84
sN Parameter: 0.89
***Angew. Chem. Int. Ed. 2013, 52, 11900-11904
DOI: 10.1002/anie.201305092
image of molecule

N-methylenepyrrolidin-1-amine (in CH2Cl2)
dichloromethaneN  Parameter: 17.90
sN Parameter: 0.48
***Angew. Chem. Int. Ed. 2013, 52, 11900-11904
DOI: 10.1002/anie.201305092
image of molecule

N-methylhydroxylamine (in MeCN)
MeCNN  Parameter: 14.10
sN Parameter: 0.76
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

N-methylindole
dichloromethaneN  Parameter: 5.75
sN Parameter: 1.23
***J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

N-methylpyrrole
dichloromethaneN  Parameter: 5.85
sN Parameter: 1.03
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

N-phenyl-1,4-dihydronicotineamide
dichloromethaneN  Parameter: 7.53
sN Parameter: 0.87
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

N-phenylcyclohexanimine (in CH2Cl2)
dichloromethaneN  Parameter: 8.80
sN Parameter: 1.00
***Z. Naturforsch. B 2013, 68b, 693-699
DOI: 10.5560/ZNB.2013-3085
image of molecule

N-phenylpropan-2-imine (in CH2Cl2)
dichloromethaneN  Parameter: 9.53
sN Parameter: 0.85
***Z. Naturforsch. B 2013, 68b, 693-699
DOI: 10.5560/ZNB.2013-3085
image of molecule

n-propanolate (in 91nPr9AN)
nPrOH-MeCN mixN  Parameter: 16.73
sN Parameter: 0.63
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

n-propanolate (in propan-1-ol)
nPrOHN  Parameter: 16.03
sN Parameter: 0.70
***Can. J. Chem. 2005, 83, 1554-1560
DOI: 10.1139%2Fv05-170
image of molecule

n-propylamine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 13.41
sN Parameter: 0.66
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

n-propylamine (in DMSO)
DMSON  Parameter: 15.70
sN Parameter: 0.64
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

n-propylamine (in MeCN)
MeCNN  Parameter: 15.11
sN Parameter: 0.63
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

n-propylamine (in water)
waterN  Parameter: 13.33
sN Parameter: 0.56
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

N-vinylcarbazole
dichloromethaneN  Parameter: 5.02
sN Parameter: 0.94
**Macromolecules 2002, 35, 5454-5458
DOI: 10.1021/ma020306l
image of molecule

NaB(OAc)3H (in DMSO)
DMSON  Parameter: 14.45
sN Parameter: 0.76
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

NaBH3(CN) (in DMSO)
DMSON  Parameter: 11.52
sN Parameter: 0.67
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

NaBH4 (in DMSO)
DMSON  Parameter: 14.74
sN Parameter: 0.81
***Angew. Chem. Int. Ed. 2009, 48, 1958-1961
DOI: 10.1002/anie.200804263
image of molecule

NADH (in water)
waterN  Parameter: 10.37
sN Parameter: 0.54
***Org. Biomol. Chem. 2023, 21, 85-88
DOI: 10.1039/D2OB02041F
image of molecule

NADPH (in water)
waterN  Parameter: 10.68
sN Parameter: 0.54
***Org. Biomol. Chem. 2023, 21, 85-88
DOI: 10.1039/D2OB02041F
image of molecule

naphthalene-2-thiolate (in DMSO)
DMSON  Parameter: 22.55
sN Parameter: 0.83
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

nicotine (in CH2Cl2)
dichloromethaneN  Parameter: 10.40
sN Parameter: 1.04
***J. Phys. Org. Chem. 2016, 29, 759-767
DOI: 10.1002/poc.3580
image of molecule

nicotine (in MeCN)
MeCNN  Parameter: 11.60
sN Parameter: 0.81
***J. Phys. Org. Chem. 2016, 29, 759-767
DOI: 10.1002/poc.3580
image of molecule

nitrite ion (in MeCN)
MeCNN  Parameter: 17.20
sN Parameter: 0.72
***Angew. Chem. Int. Ed. 2005, 44, 4623-4626
DOI: 10.1002/anie.200501274
image of molecule

norbornene
dichloromethaneN  Parameter: -0.25
sN Parameter: 1.09
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

o,o'-di-tert-butylphenolate (in DMSO)
DMSON  Parameter: 21.02
sN Parameter: 0.59
**J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

o-(trifluoromethyl)phenolate (in DMF)
DMFN  Parameter: 20.37
sN Parameter: 0.58
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

o-(trifluoromethyl)phenolate (in DMSO)
DMSON  Parameter: 18.47
sN Parameter: 0.61
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

o-(trifluoromethyl)phenolate (in MeCN)
MeCNN  Parameter: 18.39
sN Parameter: 0.69
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

O-ethyl dithiocarbonate (in MeCN)
MeCNN  Parameter: 19.30
sN Parameter: 0.69
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

O-isopropyl dithiocarbonate (in MeCN)
MeCNN  Parameter: 18.27
sN Parameter: 0.78
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

OH- (in 50/50 water/MeCN)
water-MeCN mixN  Parameter: 10.19
sN Parameter: 0.62
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

OH- (in water)
waterN  Parameter: 10.47
sN Parameter: 0.61
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

p-(tert-butyl)phenolate (in DMF)
DMFN  Parameter: 19.90
sN Parameter: 0.80
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-(tert-butyl)phenolate (in DMSO)
DMSON  Parameter: 19.67
sN Parameter: 0.79
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-(tert-butyl)phenolate (in MeCN)
MeCNN  Parameter: 21.70
sN Parameter: 0.58
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-(trifluoromethyl)phenolate (in DMF)
DMFN  Parameter: 22.05
sN Parameter: 0.53
**J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-(trifluoromethyl)phenolate (in DMSO)
DMSON  Parameter: 18.98
sN Parameter: 0.63
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-(trifluoromethyl)phenolate (in MeCN)
MeCNN  Parameter: 21.69
sN Parameter: 0.53
**J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-chlorophenolate (in DMF)
DMFN  Parameter: 19.67
sN Parameter: 0.72
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-chlorophenolate (in DMSO)
DMSON  Parameter: 20.34
sN Parameter: 0.64
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-chlorophenolate (in MeCN)
MeCNN  Parameter: 18.32
sN Parameter: 0.82
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-cyanophenolate (in DMF)
DMFN  Parameter: 17.85
sN Parameter: 0.71
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-cyanophenolate (in DMSO)
DMSON  Parameter: 18.78
sN Parameter: 0.57
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-cyanophenolate (in MeCN)
MeCNN  Parameter: 19.58
sN Parameter: 0.59
**J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-cymene
dichloromethaneN  Parameter: -2.80
sN Parameter: 0.97
*J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

p-methoxyphenolate (in DMF)
DMFN  Parameter: 19.90
sN Parameter: 0.82
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-methoxyphenolate (in DMSO)
DMSON  Parameter: 20.09
sN Parameter: 0.80
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-methoxyphenolate (in MeCN)
MeCNN  Parameter: 20.62
sN Parameter: 0.69
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-methylphenolate (in DMF)
DMFN  Parameter: 19.65
sN Parameter: 0.85
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-methylphenolate (in DMSO)
DMSON  Parameter: 19.08
sN Parameter: 0.87
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-methylphenolate (in H2O)
waterN  Parameter: 14.30
sN Parameter: 0.55
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-nitrobenzoate (in acetone)
acetoneN  Parameter: 18.74
sN Parameter: 0.68
***J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

p-nitrobenzoate (in MeCN)
MeCNN  Parameter: 15.30
sN Parameter: 0.76
***J. Am. Chem. Soc. 2008, 130, 3012-3022
DOI: 10.1021/ja0765464
image of molecule

p-nitrophenolate (in DMSO)
DMSON  Parameter: 14.32
sN Parameter: 0.77
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

p-toluenesulfonamide anion (in DMSO)
DMSON  Parameter: 17.14
sN Parameter: 0.60
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

p-toluidine (in MeCN)
MeCNN  Parameter: 13.19
sN Parameter: 0.69
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

p-toluidine (in water)
waterN  Parameter: 13.00
sN Parameter: 0.79
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

p-tosylmethyl isocyanide (TosMIC)
dichloromethaneN  Parameter: 3.50
sN Parameter: 0.76
***Angew. Chem. Int. Ed. 2007, 46, 3563-3566
DOI: 10.1002/anie.200605205
image of molecule

perhydroazepine (in water)
waterN  Parameter: 18.29
sN Parameter: 0.46
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

peroxomonosulfate (in water)
waterN  Parameter: 14.41
sN Parameter: 0.60
***Org. Lett. 2018, 20, 2816-2820
DOI: 10.1021/acs.orglett.8b00645
image of molecule

peroxy-beta-alanate
waterN  Parameter: 14.07
sN Parameter: 0.56
***Eur. J. Org. Chem. 2018, , 6010-6017
DOI: 10.1002/ejoc.201801158
image of molecule

peroxy-GABA
waterN  Parameter: 14.33
sN Parameter: 0.57
***Eur. J. Org. Chem. 2018, , 6010-6017
DOI: 10.1002/ejoc.201801158
image of molecule

peroxybenzoate (in H2O)
waterN  Parameter: 18.57
sN Parameter: 0.43
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

Ph2P(O)CH(-)CN (in DMSO)
DMSON  Parameter: 18.69
sN Parameter: 0.72
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
image of molecule

Ph2P(O)CH(-)CO2Et (in DMSO)
DMSON  Parameter: 19.20
sN Parameter: 0.69
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
image of molecule

Ph3P=C(CH3)-CO2Et
dichloromethaneN  Parameter: 13.09
sN Parameter: 0.73
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
image of molecule

Ph3P=CH-C(O)Me (in MeCN)
MeCNN  Parameter: 10.27
sN Parameter: 0.83
***J. Am. Chem. Soc. 2016, 138, 11272-11281
DOI: 10.1021/jacs.6b06264
image of molecule

Ph3P=CH-CHO (in MeCN)
MeCNN  Parameter: 9.09
sN Parameter: 0.74
***J. Am. Chem. Soc. 2016, 138, 11272-11281
DOI: 10.1021/jacs.6b06264
image of molecule

Ph3P=CH-CN
dichloromethaneN  Parameter: 12.29
sN Parameter: 0.75
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
image of molecule

Ph3P=CH-CO2Et
dichloromethaneN  Parameter: 12.79
sN Parameter: 0.77
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
image of molecule

Ph3P=CH-CO2Et (in DMSO)
DMSON  Parameter: 12.21
sN Parameter: 0.62
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
image of molecule

Ph3P=CH-COPh
dichloromethaneN  Parameter: 9.54
sN Parameter: 0.97
***J. Am. Chem. Soc. 2009, 131, 704-714
DOI: 10.1021/ja8056216
image of molecule

phenolate (in DMF)
DMFN  Parameter: 18.86
sN Parameter: 0.89
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

phenolate (in DMSO)
DMSON  Parameter: 19.86
sN Parameter: 0.71
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

phenolate (in MeCN)
MeCNN  Parameter: 18.53
sN Parameter: 0.85
***J. Org. Chem. 2019, 84, 8837-8858
DOI: 10.1021/acs.joc.9b01485
image of molecule

phenylacetylene
dichloromethaneN  Parameter: -0.04
sN Parameter: 0.77
***Angew. Chem. Int. Ed. 2014, 53, 4968-4971
DOI: 10.1002/anie.201402055
image of molecule

phenylalanine (anionic, in water)
waterN  Parameter: 14.12
sN Parameter: 0.53
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

phenyldiazomethane
dichloromethaneN  Parameter: 9.35
sN Parameter: 0.83
***Chem. Eur. J. 2003, 9, 4068-4076
DOI: 10.1002/chem.200304913
image of molecule

phenylsilane
dichloromethaneN  Parameter: 0.06
sN Parameter: 0.71
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

phenylsulfinate (in 50W50AN)
water-MeCN mixN  Parameter: 13.75
sN Parameter: 0.68
***J. Am. Chem. Soc. 2010, 132, 4796-4805
DOI: 10.1021/ja9102056
image of molecule

phenylsulfinate (in DMSO)
DMSON  Parameter: 19.60
sN Parameter: 0.60
***J. Am. Chem. Soc. 2010, 132, 4796-4805
DOI: 10.1021/ja9102056
image of molecule

phenylsulfinate (in MeCN)
MeCNN  Parameter: 20.11
sN Parameter: 0.59
***J. Am. Chem. Soc. 2010, 132, 4796-4805
DOI: 10.1021/ja9102056
image of molecule

phthalimide anion (in DMSO)
DMSON  Parameter: 15.52
sN Parameter: 0.67
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

phthalimidoperoxyhexanoate (in H2O)
waterN  Parameter: 16.02
sN Parameter: 0.54
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

piperazine (in water)
waterN  Parameter: 17.22
sN Parameter: 0.50
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

piperidin-1-yl dithiocarbamate (in MeCN)
MeCNN  Parameter: 23.84
sN Parameter: 0.57
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

piperidine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 15.63
sN Parameter: 0.64
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

piperidine (in DMSO)
DMSON  Parameter: 17.19
sN Parameter: 0.71
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

piperidine (in MeCN)
MeCNN  Parameter: 17.35
sN Parameter: 0.68
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

piperidine (in water)
waterN  Parameter: 18.13
sN Parameter: 0.44
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

potassium (1-(tert-butoxycarbonyl)-1H-indol-2-yl)trifluoroborate
MeCNN  Parameter: 6.46
sN Parameter: 0.96
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

potassium (1-(tert-butoxycarbonyl)-1H-indol-3-yl)trifluoroborate
MeCNN  Parameter: 4.06
sN Parameter: 0.79
**J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

potassium (1-(tert-butoxycarbonyl)-5-methoxy-1H-indol-2-yl)trifluoroborate
MeCNN  Parameter: 7.10
sN Parameter: 1.18
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

potassium allyltrifluoroborate (in MeCN)
MeCNN  Parameter: 5.29
sN Parameter: 0.87
**J. Am. Chem. Soc. 2017, 139, 15324-15327
DOI: 10.1021/jacs.7b10240
image of molecule

potassium indenide (in DMSO)
DMSON  Parameter: 24.16
sN Parameter: 0.68
***Angew. Chem. Int. Ed. 2015, 54, 12497-12500
DOI: 10.1002/anie.201501385
image of molecule

potassium trifluoro(1-methyl-1H-indol-2-yl)borate
MeCNN  Parameter: 9.55
sN Parameter: 1.16
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

potassium trifluoro(1-methyl-1H-indol-5-yl)borate
MeCNN  Parameter: 8.77
sN Parameter: 1.09
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

potassium trifluoro(3-methoxy-thiophen-2-yl)borate
MeCNN  Parameter: 7.32
sN Parameter: 0.90
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

potassium trifluoro(furan-3-yl)borate
MeCNN  Parameter: 6.83
sN Parameter: 0.93
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

prenyl-tributylstannane
dichloromethaneN  Parameter: 4.74
sN Parameter: 1.15
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

prolinate (in MeCN)
MeCNN  Parameter: 19.95
sN Parameter: 0.68
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

proline (anionic, in water)
waterN  Parameter: 18.08
sN Parameter: 0.50
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

propargylamine (in water)
waterN  Parameter: 12.29
sN Parameter: 0.59
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

propene
dichloromethaneN  Parameter: -2.41
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

purine anion (in DMSO)
DMSON  Parameter: 15.03
sN Parameter: 0.77
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

purine anion (in water)
waterN  Parameter: 11.00
sN Parameter: 0.54
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

pyridine (in CH2Cl2)
dichloromethaneN  Parameter: 12.90
sN Parameter: 0.67
*Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

pyridine (in H2O)
waterN  Parameter: 11.05
sN Parameter: 0.73
***Chem. Eur. J. 2007, 13, 336-345
DOI: 10.1002/chem.200600941
image of molecule

pyridine (in MeCN)
MeCNN  Parameter: 13.60
sN Parameter: 0.60
***Synthesis 2017, 49, 3495-3504
DOI: 10.1055/s-0036-1590504
image of molecule

pyrrole
dichloromethaneN  Parameter: 4.63
sN Parameter: 1.00
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

pyrrolidin-1-yl dithiocarbamate (in MeCN)
MeCNN  Parameter: 22.40
sN Parameter: 0.63
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

pyrrolidine (in 91M9AN)
MeOH-MeCN mixN  Parameter: 15.97
sN Parameter: 0.63
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

pyrrolidine (in water)
waterN  Parameter: 17.21
sN Parameter: 0.49
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

pyrrolidine (inMeCN)
MeCNN  Parameter: 18.58
sN Parameter: 0.61
***J. Am. Chem. Soc. 2020, 142, 1526-1547
DOI: 10.1021/jacs.9b11877
image of molecule

quinidine
dichloromethaneN  Parameter: 10.54
sN Parameter: 0.74
***J. Org. Chem. 2009, 74, 7157-7164
DOI: 10.1021/jo901670w
image of molecule

quinine
dichloromethaneN  Parameter: 10.46
sN Parameter: 0.75
***J. Org. Chem. 2009, 74, 7157-7164
DOI: 10.1021/jo901670w
image of molecule

quinuclidine (in MeCN)
MeCNN  Parameter: 20.54
sN Parameter: 0.60
***Angew. Chem. Int. Ed. 2007, 46, 6176-6179
DOI: 10.1002/anie.200701489
image of molecule

saccharin anion (in MeCN)
MeCNN  Parameter: 10.78
sN Parameter: 0.89
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

semicarbazide (in water)
waterN  Parameter: 11.05
sN Parameter: 0.52
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

serine (anionic, in water)
waterN  Parameter: 13.16
sN Parameter: 0.55
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

SO3(2-) (in water)
waterN  Parameter: 16.83
sN Parameter: 0.56
***J. Am. Chem. Soc. 2003, 125, 286-295
DOI: 10.1021/ja021010y
image of molecule

sodium indenide (in DMSO)
DMSON  Parameter: 23.74
sN Parameter: 0.71
***Angew. Chem. Int. Ed. 2015, 54, 12497-12500
DOI: 10.1002/anie.201501385
image of molecule

styrene
dichloromethaneN  Parameter: 0.78
sN Parameter: 0.95
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

succinimide anion (in DMSO)
DMSON  Parameter: 16.03
sN Parameter: 0.66
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

t-butylperoxy anion (in H2O)
waterN  Parameter: 14.29
sN Parameter: 0.51
***Angew. Chem. Int. Ed. 2017, 56, 13279-13282
DOI: 10.1002/anie.201707086
image of molecule

TCAP (in MeCN)
MeCNN  Parameter: 15.60
sN Parameter: 0.68
***Chem. Eur. J. 2013, 19, 6435-6442
DOI: 10.1002/chem.201204452
image of molecule

tert-butanol (in MeCN)
MeCNN  Parameter: 5.35
sN Parameter: 0.72
***Bull. Chem. Soc. Jpn. 2018, 91, 523-530
DOI: 10.1246/bcsj.20170360
image of molecule

tert-butyl hydrazinecarboxylate (in MeCN)
MeCNN  Parameter: 11.40
sN Parameter: 0.70
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

tert-butyl indole-1-carboxylate
MeCNN  Parameter: 1.68
sN Parameter: 1.26
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

tert-butyl isocyanide
dichloromethaneN  Parameter: 5.47
sN Parameter: 0.77
***Angew. Chem. Int. Ed. 2007, 46, 3563-3566
DOI: 10.1002/anie.200605205
image of molecule

tert-butylamine (in MeCN)
MeCNN  Parameter: 12.35
sN Parameter: 0.72
***Eur. J. Org. Chem. 2009, , 6379-6385
DOI: 10.1002/ejoc.200900925
image of molecule

tert-butylamine (in water)
waterN  Parameter: 10.48
sN Parameter: 0.65
***J. Org. Chem. 2007, 72, 3679-3688
DOI: 10.1021/jo062586z
image of molecule

tetra-sec.butylstannane (in 1,2-DCE)
1,2-dichloroethaneN  Parameter: -1.10
sN Parameter: 1.15
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetrabutylstannane
dichloromethaneN  Parameter: -0.30
sN Parameter: 1.07
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetraethylgermane (in MeCN)
MeCNN  Parameter: -4.70
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetraethylplumbane (in MeCN)
MeCNN  Parameter: 0.10
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetraethylsilane
MeCNN  Parameter: -6.50
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetraethylstannane (in 1,2-DCE)
1,2-dichloroethaneN  Parameter: -1.90
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetraethylstannane (in MeCN)
MeCNN  Parameter: -2.40
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetrahydroborate ion (in water)
waterN  Parameter: 12.10
sN Parameter: 0.79
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetrahydrofuran (in dichloromethane)
dichloromethaneN  Parameter: -3.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetrahydrothiophene (in CH2Cl2)
dichloromethaneN  Parameter: 13.10
sN Parameter: 0.72
-Chem. Eur. J. 2021, 21, 11367-11376
DOI: 10.1002/chem.202100977
image of molecule

tetrahydrothiophene (in MeCN)
MeCNN  Parameter: 13.30
sN Parameter: 0.72
-Chem. Eur. J. 2021, 21, 11367-11376
DOI: 10.1002/chem.202100977
image of molecule

tetrahydrothiopyran (in CH2Cl2)
dichloromethaneN  Parameter: 11.94
sN Parameter: 0.75
**Chem. Eur. J. 2021, 21, 11367-11376
DOI: 10.1002/chem.202100977
image of molecule

tetraisobutylstannane
dichloromethaneN  Parameter: 1.35
sN Parameter: 1.10
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tetrakis(5-methyl-furan-2-yl)borate
MeCNN  Parameter: 9.09
sN Parameter: 1.12
***Chem. Sci. 2012, 3, 878-882
DOI: 10.1039/c2sc00883a
image of molecule

tetramethylethylene
dichloromethaneN  Parameter: -1.00
sN Parameter: 1.40
***Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

tetrapropylstannane (in 1,2-DCE)
1,2-dichloroethaneN  Parameter: -0.50
sN Parameter: 1.13
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

theophylline anion (in DMSO)
DMSON  Parameter: 14.78
sN Parameter: 0.71
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

theophylline anion (in water)
waterN  Parameter: 10.06
sN Parameter: 0.71
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

thioacetate (in MeCN)
MeCNN  Parameter: 21.20
sN Parameter: 0.63
***Org. Biomol. Chem. 2011, 9, 8046-8050
DOI: 10.1039/c1ob06245j
image of molecule

thiocyanate (in MeCN)
MeCNN  Parameter: 17.94
sN Parameter: 0.60
***J. Am. Chem. Soc. 2003, 125, 14126-14132
DOI: 10.1021/ja037317u
image of molecule

thiocyanate (in MeCN)
MeCNN  Parameter: 12.13
sN Parameter: 0.60
*J. Am. Chem. Soc. 2003, 125, 14126-14132
DOI: 10.1021/ja037317u
image of molecule

thiophene
dichloromethaneN  Parameter: -1.01
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

thiophenolate (in DMSO)
DMSON  Parameter: 23.36
sN Parameter: 0.74
***J. Org. Chem. 2021, 86, 5965-5972
DOI: 10.1021/acs.joc.1c00025
image of molecule

threonine (anionic, in water)
waterN  Parameter: 12.69
sN Parameter: 0.60
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

THTP (3,5,6,7-tetrahydro-2H-thiazolo[3,2-a]pyrimidine)
dichloromethaneN  Parameter: 14.45
sN Parameter: 0.78
***J. Org. Chem. 2011, 76, 5104-5112
DOI: 10.1021/jo200803x
image of molecule

thymine anion (in DMSO)
DMSON  Parameter: 17.63
sN Parameter: 0.62
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

thymine anion (in water)
waterN  Parameter: 11.17
sN Parameter: 0.51
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

toluene
dichloromethaneN  Parameter: -4.36
sN Parameter: 1.77
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

trans-HMo(CO)2(PCy3)Cp
dichloromethaneN  Parameter: 6.50
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trans-HMo(CO)2(PMe3)Cp
dichloromethaneN  Parameter: 7.80
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trans-HMo(CO)2(PPh3)Cp
dichloromethaneN  Parameter: 6.60
sN Parameter: 0.80
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tri-n-butylphosphane
dichloromethaneN  Parameter: 15.49
sN Parameter: 0.69
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

tri-p-tolylmethane
dichloromethaneN  Parameter: -3.62
sN Parameter: 0.80
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tri-p-tolylmethane (in MeCN)
MeCNN  Parameter: -8.80
sN Parameter: 0.82
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tributyl phosphite
dichloromethaneN  Parameter: 10.36
sN Parameter: 0.70
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

tributylgermane
dichloromethaneN  Parameter: 5.92
sN Parameter: 0.73
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

tributylsilane
dichloromethaneN  Parameter: 3.99
sN Parameter: 0.73
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tributylstannane
dichloromethaneN  Parameter: 9.96
sN Parameter: 0.55
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

tricyclohexylphosphane
dichloromethaneN  Parameter: 14.64
sN Parameter: 0.68
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

triethoxysilane
dichloromethaneN  Parameter: -1.80
sN Parameter: 0.75
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

triethylamine (in CH2Cl2)
dichloromethaneN  Parameter: 17.30
sN Parameter: 0.52
*J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

triethylamine (in MeCN)
MeCNN  Parameter: 17.10
sN Parameter: 0.52
*J. Phys. Org. Chem. 2010, 23, 1029-1035
DOI: 10.1002/poc.1707
image of molecule

triethylgermane
dichloromethaneN  Parameter: 4.00
sN Parameter: 0.75
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

triethylsilane
dichloromethaneN  Parameter: 3.58
sN Parameter: 0.70
***J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

trifluoroacetamide anion (in DMSO)
DMSON  Parameter: 15.81
sN Parameter: 0.64
***J. Org. Chem. 2010, 75, 5250-5258
DOI: 10.1021/jo1009883
image of molecule

trifluoroethanol
TFEN  Parameter: 1.11
sN Parameter: 0.96
***J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

trihexylsilane
dichloromethaneN  Parameter: 3.89
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

triisopropylphosphane
dichloromethaneN  Parameter: 13.37
sN Parameter: 0.70
*Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

triisopropylsilane
dichloromethaneN  Parameter: 2.93
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl phosphite (in 91M9AN)
MeOH-MeCN mixN  Parameter: 9.04
sN Parameter: 0.70
***Angew. Chem. Int. Ed. 2006, 45, 3869-3874
DOI: 10.1002/anie.200600542
image of molecule

trimethyl(3-(trimethylgermyl)propyl)silane (in MeCN)
MeCNN  Parameter: -4.80
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(3-(trimethylplumbyl)propyl)germane (in MeCN)
MeCNN  Parameter: -1.00
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(3-(trimethylplumbyl)propyl)silane (in MeCN)
MeCNN  Parameter: -1.20
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(3-(trimethylstannyl)propyl)germane (in MeCN)
MeCNN  Parameter: -2.40
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(3-(trimethylstannyl)propyl)silane (in MeCN)
MeCNN  Parameter: -3.40
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(4-methylphenethyl)stannane
1,2-dichloroethaneN  Parameter: -0.50
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(phenethyl)silane
dichloromethaneN  Parameter: -3.50
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(phenethyl)stannane
1,2-dichloroethaneN  Parameter: -1.10
sN Parameter: 1.10
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

trimethyl(prenyl)silane
dichloromethaneN  Parameter: 0.90
sN Parameter: 1.17
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

trimethylamine (in MeCN)
MeCNN  Parameter: 23.05
sN Parameter: 0.45
***J. Org. Chem. 2012, 77, 8142-8155
DOI: 10.1021/jo301497g
image of molecule

trimethylhydrazine (in MeCN)
MeCNN  Parameter: 12.43
sN Parameter: 0.75
***Angew. Chem. Int. Ed. 2012, 51, 1353-1356
DOI: 10.1002/anie.201107315
image of molecule

trimethylhydrazine (in MeCN)
MeCNN  Parameter: 17.75
sN Parameter: 0.53
***Angew. Chem. Int. Ed. 2012, 51, 1353-1356
DOI: 10.1002/anie.201107315
image of molecule

trimethylsilane
dichloromethaneN  Parameter: 3.15
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

triphenyl phosphite
dichloromethaneN  Parameter: 5.51
sN Parameter: 0.76
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

triphenylgermane
dichloromethaneN  Parameter: 3.99
sN Parameter: 0.62
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

triphenylmethane
dichloromethaneN  Parameter: -4.27
sN Parameter: 0.80
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

triphenylphosphane
dichloromethaneN  Parameter: 14.33
sN Parameter: 0.65
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

triphenylphosphine (in THF)
THFN  Parameter: 13.59
sN Parameter: 0.66
***Angew. Chem. Int. Ed. 2011, 50, 6915-6919
DOI: 10.1002/anie.201102435
image of molecule

triphenylsilane
dichloromethaneN  Parameter: 2.65
sN Parameter: 0.72
***Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

triphenylstannane
dichloromethaneN  Parameter: 5.64
sN Parameter: 0.59
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

tripropylsilane
dichloromethaneN  Parameter: 3.67
sN Parameter: 0.73
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tris((butyldimethylsilyl)methyl)silane
dichloromethaneN  Parameter: 3.73
sN Parameter: 0.68
**Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tris((dimethyl(phenyl)silyl)methyl)silane
dichloromethaneN  Parameter: 3.40
sN Parameter: 0.66
**Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tris((trimethylsilyl)methyl)silane
dichloromethaneN  Parameter: 3.59
sN Parameter: 0.67
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tris(2,4-dimethylphenyl)phosphane
dichloromethaneN  Parameter: 14.88
sN Parameter: 0.41
-Chem. Eur. J. 2017, 23, 7422-7427
DOI: 10.1002/chem.201701080
image of molecule

tris(2,6-dimethoxyphenyl)phosphane
dichloromethaneN  Parameter: 15.19
sN Parameter: 0.88
-Chem. Eur. J. 2017, 23, 7422-7427
DOI: 10.1002/chem.201701080
image of molecule

tris(2,6-dimethoxyphenyl)phosphane (in MeCN)
MeCNN  Parameter: 18.11
sN Parameter: 0.62
-Chem. Eur. J. 2017, 23, 7422-7427
DOI: 10.1002/chem.201701080
image of molecule

tris(2-methoxyphenyl)phosphane
dichloromethaneN  Parameter: 14.26
sN Parameter: 0.73
-Chem. Eur. J. 2017, 23, 7422-7427
DOI: 10.1002/chem.201701080
image of molecule

tris(2-methylphenyl)phosphane
dichloromethaneN  Parameter: 8.56
sN Parameter: 0.70
-Chem. Eur. J. 2017, 23, 7422-7427
DOI: 10.1002/chem.201701080
image of molecule

tris(4-(dimethylamino)phenyl)methane (in MeCN)
MeCNN  Parameter: -3.30
sN Parameter: 0.82
-Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tris(4-chlorophenyl)phosphane
dichloromethaneN  Parameter: 12.58
sN Parameter: 0.65
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

tris(4-dimethylaminophenyl)phosphane
dichloromethaneN  Parameter: 18.39
sN Parameter: 0.64
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

tris(4-methoxyphenyl)methane (in MeCN)
MeCNN  Parameter: -5.18
sN Parameter: 0.82
*Chem. Eur. J. 2013, 19, 249-263
DOI: 10.1002/chem.201202839
image of molecule

tris(4-methoxyphenyl)phosphane
dichloromethaneN  Parameter: 16.17
sN Parameter: 0.62
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

tris(4-methylphenyl)phosphane
dichloromethaneN  Parameter: 15.44
sN Parameter: 0.64
***Chem. Eur. J. 2005, 11, 917-927
DOI: 10.1002/chem.200400696
image of molecule

uracil anion (in DMSO)
DMSON  Parameter: 17.04
sN Parameter: 0.63
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

uracil anion (in water)
waterN  Parameter: 10.75
sN Parameter: 0.53
***Chem. Eur. J. 2012, 18, 127-137
DOI: 10.1002/chem.201102411
image of molecule

valine (anionic, in water)
waterN  Parameter: 13.65
sN Parameter: 0.57
***Org. Biomol. Chem. 2007, 5, 3814-3820
DOI: 10.1039/b713778h
image of molecule

water (in MeCN)
MeCNN  Parameter: 5.79
sN Parameter: 0.72
***Bull. Chem. Soc. Jpn. 2018, 91, 523-530
DOI: 10.1246/bcsj.20170360
image of molecule

xanthene
dichloromethaneN  Parameter: 0.64
sN Parameter: 0.97
*J. Am. Chem. Soc. 2002, 124, 4076-4083
DOI: 10.1021/ja0121538
image of molecule

Z-3-(trimethylsiloxy)pent-2-ene
dichloromethaneN  Parameter: 5.58
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

[H-B(2,4,6-F3C6H2)3]- [NEt4]+
MeCNN  Parameter: 14.13
sN Parameter: 0.61
***Angew. Chem. Int. Ed. 2015, 54, 14508-14512
DOI: 10.1002/anie.201507298
image of molecule

[H-B(2,6-F2C6H3)3]- [NEt4]+
MeCNN  Parameter: 13.97
sN Parameter: 0.66
***Angew. Chem. Int. Ed. 2015, 54, 14508-14512
DOI: 10.1002/anie.201507298
image of molecule

[H-B(C6F5)3]- [NEt4]+
MeCNN  Parameter: 10.04
sN Parameter: 0.73
***Angew. Chem. Int. Ed. 2015, 54, 14508-14512
DOI: 10.1002/anie.201507298