Mayr's Database of Reactivity Parameters

N-Nucleophiles

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Name Solvent Reactivity
Parameters
Classification Reference
(title or year)
4-(dimethylamino)pyridine (in CH2Cl2)
C7H10N2 *
dichloromethane

N  Param.: 15.80

sN Param.: 0.66
*** Chem. Eur. J. 2007, 13, 336-345
10.1002/chem.200600941
trifluoroacetamide anion (in DMSO)
*
DMSO

N  Param.: 15.81

sN Param.: 0.64
*** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
Se-HyperBTM (in MeCN)
C19H20N2Se *
MeCN

N  Param.: 15.84

sN Param.: 0.57
*** Angew. Chem. Int. Ed. 2025, 64, e202514865
10.1002/anie.202514865
4-pyrrolidinopyridine (in CH2Cl2)
C9H12N2 *
dichloromethane

N  Param.: 15.90

sN Param.: 0.67
* Chem. Eur. J. 2007, 13, 336-345
10.1002/chem.200600941
4-(dimethylamino)pyridine (in THF)
*
THF

N  Param.: 15.90

sN Param.: 0.66
*** Angew. Chem. Int. Ed. 2011, 50, 6915-6919
10.1002/anie.201102435
(S)-2-(pyrrolidin-2-ylmethyl)isoindoline-1,3-dione
C13H14N2O2 *
MeCN

N  Param.: 15.90

sN Param.: 0.77
*** J. Am. Chem. Soc. 2020, 142, 1526-1547
10.1021/jacs.9b11877
pyrrolidine (in 91M9AN)
C4H9N *
MeOH-MeCN mix

N  Param.: 15.97

sN Param.: 0.63
*** Angew. Chem. Int. Ed. 2006, 45, 3869-3874
10.1002/anie.200600542
ethyl N-acetylcarbamate anion (in DMSO)
*
DMSO

N  Param.: 15.99

sN Param.: 0.70
*** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
succinimide anion (in DMSO)
*
DMSO

N  Param.: 16.03

sN Param.: 0.66
*** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
diacetamide anion (in DMSO)
*
DMSO

N  Param.: 16.05

sN Param.: 0.70
*** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
2-formyl-imidazole anion (in DMSO)
*
DMSO

N  Param.: 16.06

sN Param.: 0.68
*** Chem. Eur. J. 2012, 18, 127-137
10.1002/chem.201102411
ethanolamine (in DMSO)
*
DMSO

N  Param.: 16.07

sN Param.: 0.61
*** J. Am. Chem. Soc. 2009, 131, 11392-11401
10.1021/ja903207b
Se-HyperBTM (in DCM)
C19H20N2Se *
dichloromethane

N  Param.: 16.11

sN Param.: 0.58
*** Angew. Chem. Int. Ed. 2025, 64, e202514865
10.1002/anie.202514865
DBU (in THF)
*
THF

N  Param.: 16.12

sN Param.: 0.67
*** Angew. Chem. Int. Ed. 2011, 50, 6915-6919
10.1002/anie.201102435
1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyrimidine (TBN)
C6H11N3 *
dichloromethane

N  Param.: 16.15

sN Param.: 0.73
*** ChemCatChem 2012, 4, 993-999
10.1002/cctc.201200143
1,2-dimethylhydrazine (in MeCN)
*
MeCN

N  Param.: 16.15

sN Param.: 0.68
*** J. Org. Chem. 2012, 77, 8142-8155
10.1021/jo301497g
2,3,4,6,7,8-hexahydro-1H-pyrimido[1,2-a]pyrimidine
C7H13N3 *
dichloromethane

N  Param.: 16.16

sN Param.: 0.75
*** ChemCatChem 2012, 4, 993-999
10.1002/cctc.201200143
(S)-diphenyl(pyrrolidin-2-yl)methanol
C17H19NO *
MeCN

N  Param.: 16.18

sN Param.: 0.56
*** J. Am. Chem. Soc. 2020, 142, 1526-1547
10.1021/jacs.9b11877
DBN (in MeCN)
C7H12N2 *
MeCN

N  Param.: 16.28

sN Param.: 0.67
*** Chem. Commun. 2008, , 1792-1794
10.1039/b801811a
benzotriazole anion (in DMSO)
*
DMSO

N  Param.: 16.29

sN Param.: 0.65
*** Chem. Eur. J. 2012, 18, 127-137
10.1002/chem.201102411
azide ion (in 91E9AN)
N3- *
EtOH-MeCN mix

N  Param.: 16.30

sN Param.: 0.73
*** J. Phys. Org. Chem. 2006, 19, 706-713
10.1002/poc.1063
1-methyl uracil anion (in DMSO)
*
DMSO

N  Param.: 16.36

sN Param.: 0.69
*** Chem. Eur. J. 2012, 18, 127-137
10.1002/chem.201102411
pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Ph4P+) (in MeCN)
C6H4F3N2O2S- *
MeCN

N  Param.: 16.38

sN Param.: 0.60
*** J. Am. Chem. Soc. 2025, 147, 5043-5050
10.1021/jacs.4c14825
4-formyl-imidazole anion (in DMSO)
*
DMSO

N  Param.: 16.40

sN Param.: 0.67
*** Chem. Eur. J. 2012, 18, 127-137
10.1002/chem.201102411
(R)-2-isopropylpyrrolidine
C7H15N *
MeCN

N  Param.: 16.44

sN Param.: 0.71
*** J. Am. Chem. Soc. 2020, 142, 1526-1547
10.1021/jacs.9b11877
hydrazine (in MeCN)
*
MeCN

N  Param.: 16.45

sN Param.: 0.56
*** Angew. Chem. Int. Ed. 2012, 51, 1353-1356
10.1002/anie.201107315
pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Bu4P+) (in MeCN)
C6H4F3N2O2S- *
MeCN

N  Param.: 16.48

sN Param.: 0.60
*** J. Org. Chem. 2025, 90, 2298-2306
10.1021/acs.joc.4c02668
N-methyl-morpholine (in CH2Cl2)
*
dichloromethane

N  Param.: 16.50

sN Param.: 0.52
* J. Phys. Org. Chem. 2010, 23, 1029-1035
10.1002/poc.1707
(R)-2-isopropyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
*
dichloromethane

N  Param.: 16.50

sN Param.: 0.48
*** J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
(S)-2-(methoxymethyl)pyrrolidine
C6H13NO *
MeCN

N  Param.: 16.50

sN Param.: 0.71
*** J. Am. Chem. Soc. 2020, 142, 1526-1547
10.1021/jacs.9b11877
(S)-2-benzhydrylpyrrolidine
C17H19N *
MeCN

N  Param.: 16.61

sN Param.: 0.67
*** J. Am. Chem. Soc. 2020, 142, 1526-1547
10.1021/jacs.9b11877
Te-DHPB (in CH2Cl2)
C10H10N2Te *
dichloromethane

N  Param.: 16.63

sN Param.: 0.65
*** Angew. Chem. Int. Ed. 2025, 64, e202514865
10.1002/anie.202514865
Te-HyperBTM (in DCM)
C19H20N2Te *
dichloromethane

N  Param.: 16.63

sN Param.: 0.63
*** ChemistryEurope 2026, 4, e202500443
10.1002/ceur.202500443
2-Me super-dmap (in MeCN)
*
MeCN

N  Param.: 16.65

sN Param.: 0.58
*** Org. Lett. 2011, 13, 530-533
10.1021/ol1029589
pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Bu4N+) (in MeCN)
C6H4F3N2O2S- *
MeCN

N  Param.: 16.68

sN Param.: 0.59
*** J. Org. Chem. 2025, 90, 2298-2306
10.1021/acs.joc.4c02668
azide ion (in 91nPr9AN)
N3- *
nPrOH-MeCN mix

N  Param.: 16.70

sN Param.: 0.73
*** J. Phys. Org. Chem. 2006, 19, 706-713
10.1002/poc.1063
(S)-pyrrolidin-2-ylmethanol
C5H11NO *
MeCN

N  Param.: 16.74

sN Param.: 0.67
*** J. Am. Chem. Soc. 2020, 142, 1526-1547
10.1021/jacs.9b11877
2-methylpyrrolidine (in MeCN)
C5H11N *
MeCN

N  Param.: 16.78

sN Param.: 0.71
*** J. Am. Chem. Soc. 2020, 142, 1526-1547
10.1021/jacs.9b11877
N-methyl-morpholine (in MeCN)
*
MeCN

N  Param.: 16.80

sN Param.: 0.52
* J. Phys. Org. Chem. 2010, 23, 1029-1035
10.1002/poc.1707
1-methyl-2-phenylpyrrolidine (in CH2Cl2)
C11H15N *
dichloromethane

N  Param.: 16.80

sN Param.: 0.49
*** J. Phys. Org. Chem. 2016, 29, 759-767
10.1002/poc.3580
2-Et super-dmap (in MeCN)
*
MeCN

N  Param.: 16.81

sN Param.: 0.60
*** Org. Lett. 2011, 13, 530-533
10.1021/ol1029589
morpholine (in DMSO)
C4H9NO *
DMSO

N  Param.: 16.96

sN Param.: 0.67
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
uracil anion (in DMSO)
*
DMSO

N  Param.: 17.04

sN Param.: 0.63
*** Chem. Eur. J. 2012, 18, 127-137
10.1002/chem.201102411
azide ion (in 91iPr9AN)
N3- *
iPrOH-MeCN mix

N  Param.: 17.07

sN Param.: 0.71
*** J. Phys. Org. Chem. 2006, 19, 706-713
10.1002/poc.1063
triethylamine (in MeCN)
*
MeCN

N  Param.: 17.10

sN Param.: 0.52
* J. Phys. Org. Chem. 2010, 23, 1029-1035
10.1002/poc.1707
dimethylamine (in water)
C2H7N *
water

N  Param.: 17.12

sN Param.: 0.50
*** J. Org. Chem. 2007, 72, 3679-3688
10.1021/jo062586z
p-toluenesulfonamide anion (in DMSO)
*
DMSO

N  Param.: 17.14

sN Param.: 0.60
*** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
piperidine (in DMSO)
C5H11N *
DMSO

N  Param.: 17.19

sN Param.: 0.71
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
pyridin-4-yl(tosyl)amide (Ph4P+) (in MeCN)
C12H11N2O2S- *
MeCN

N  Param.: 17.19

sN Param.: 0.64
*** J. Org. Chem. 2025, 90, 2298-2306
10.1021/acs.joc.4c02668
nitrite ion (in MeCN)
NO2 *
MeCN

N  Param.: 17.20

sN Param.: 0.72
*** Angew. Chem. Int. Ed. 2005, 44, 4623-4626
10.1002/anie.200501274