Mayr's Database of Reactivity Parameters

C-Nucleophiles

For reactivities of structurally related compounds go to: Nucleophiles
1 | 2 | 3 | 4 | 5 | 6 Found 572 molecules, displaying page 5 of 6 Results per page 10|50|100|all
Name Solvent Reactivity
Parameters 		Classification Reference
(title or year)
anion of nitromethane (in DMSO)
CH2NO2-*
 DMSO

N  Param.: 20.71

sN Param.: 0.60		***J. Org. Chem. 2004, 69, 7565-7576
10.1021/jo048773j
anion of nitromethane (in water)
CH2NO2-*
 water

N  Param.: 12.06

sN Param.: 0.53		***J. Org. Chem. 2004, 69, 7565-7576
10.1021/jo048773j
anion of p-tolylnitromethane (in 91M9AN)
C8H8NO2-*
 MeOH-MeCN mix

N  Param.: 13.58

sN Param.: 0.64		***Eur. J. Org. Chem. 2006, , 2530-2537
10.1002/ejoc.200500769
anion of p-tolylnitromethane (in DMSO)
C8H8NO2-*
 DMSO

N  Param.: 18.31

sN Param.: 0.76		***J. Org. Chem. 2004, 69, 7565-7576
10.1021/jo048773j
anion of p-tolylnitromethane (in water)
C8H8NO2-*
 water

N  Param.: 13.09

sN Param.: 0.50		***J. Org. Chem. 2004, 69, 7565-7576
10.1021/jo048773j
anion of phenylnitromethane (in 91M9AN)
C7H6NO2-*
 MeOH-MeCN mix

N  Param.: 12.51

sN Param.: 0.67		***Eur. J. Org. Chem. 2006, , 2530-2537
10.1002/ejoc.200500769
anion of phenylnitromethane (in DMSO)
C7H6NO2-*
 DMSO

N  Param.: 18.29

sN Param.: 0.71		***J. Org. Chem. 2004, 69, 7565-7576
10.1021/jo048773j
anion of phenylnitromethane (in H2O)
C7H6NO2-*
 water

N  Param.: 12.05

sN Param.: 0.53		***J. Org. Chem. 2004, 69, 7565-7576
10.1021/jo048773j
anion of triethyl methanetricarboxylate (in DMSO)
C10H15O6*
 DMSO

N  Param.: 15.33

sN Param.: 0.72		***Eur. J. Org. Chem. 2016, , 1841-1848
10.1002/ejoc.201600107
anisole
C7H8O*
 dichloromethane

N  Param.: -1.18

sN Param.: 1.20		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
azulene
C10H8*
 MeCN

N  Param.: 6.66

sN Param.: 1.02		***Eur. J. Org. Chem. 2009, , 1202-1206
10.1002/ejoc.200801099
barbiturate anion (in DMSO)
C4H3N2O3*
 DMSO

N  Param.: 15.59

sN Param.: 0.80		***J. Org. Chem. 2017, 82, 8476-8488
10.1021/acs.joc.7b01223
benzyl (1-phenylvinyl)carbamate
C16H15NO2*
 MeCN

N  Param.: 6.21

sN Param.: 0.87		***Chem. Eur. J. 2012, 18, 5732-5740
10.1002/chem.201103519
benzyl isocyanide
C8H7N*
 dichloromethane

N  Param.: 4.90

sN Param.: 0.74		***Angew. Chem. Int. Ed. 2007, 46, 3563-3566
10.1002/anie.200605205
beta-(trimethylsilyl)styrene
C11H16Si*
 dichloromethane

N  Param.: -0.43

sN Param.: 1.06		***Chem. Eur. J. 2014, 20, 1103-1110
10.1002/chem.201303215
bis(4-nitrophenyl)methanide (in DMSO)
C13H9N2O4-*
 DMSO

N  Param.: 19.92

sN Param.: 0.67		***ARKIVOC 2008, (x), 37-53
10.3998/ark.5550190.[...]
bis(phenylsulfonyl)methanide (in DMSO)
C13H11O4S2*
 DMSO

N  Param.: 15.68

sN Param.: 0.74		***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
10.1002/anie.201605616
bromo(phenylsulfonyl)methanide (in DMSO)
C7H6BrO2S*
 DMSO

N  Param.: 23.90

sN Param.: 0.62		***J. Org. Chem. 2017, 82, 2011-2017
10.1021/acs.joc.6b02844
buta-1,3-diene
C4H6*
 dichloromethane

N  Param.: -0.87

sN Param.: 1.00		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
chloro((4-chlorophenyl)sulfonyl)methanide (in DMSO)
C7H5Cl2O2S*
 DMSO

N  Param.: 26.90

sN Param.: 0.45		***J. Org. Chem. 2017, 82, 2011-2017
10.1021/acs.joc.6b02844
chloro((4-cyanophenyl)sulfonyl)methanide (in DMSO)
C8H5ClNO2S*
 DMSO

N  Param.: 25.59

sN Param.: 0.51		***J. Org. Chem. 2017, 82, 2011-2017
10.1021/acs.joc.6b02844
chloro((4-nitrophenyl)sulfonyl)methanide (in DMSO)
C7H5ClNO4S*
 DMSO

N  Param.: 24.88

sN Param.: 0.49		***J. Org. Chem. 2017, 82, 2011-2017
10.1021/acs.joc.6b02844
chloro(phenylsulfonyl)methanide (in DMF)
C7H6ClO2S *
 DMF

N  Param.: 26.64

sN Param.: 0.64		-Chem. Eur. J. 2008, 14, 6108-6118
10.1002/chem.200800329
chloro(phenylsulfonyl)methanide (in DMSO)
C7H6ClO2S*
 DMSO

N  Param.: 28.27

sN Param.: 0.42		***J. Org. Chem. 2017, 82, 2011-2017
10.1021/acs.joc.6b02844
Cp2Ti(CH2Ph)2 - Dibenzyltitanocene
*
 dichloromethane

N  Param.: 4.38

sN Param.: 1.00		*Chem. Eur. J. 2016, 22, 11196-11200
10.1002/chem.201602452
Cp2Zr(CH2Ph)2 - Dibenzylzirconocene
*
 dichloromethane

N  Param.: 5.10

sN Param.: 1.03		***Chem. Eur. J. 2016, 22, 11196-11200
10.1002/chem.201602452
Cp2Zr(Me)2 - Dimethylzirconocene
*
 dichloromethane

N  Param.: 4.35

sN Param.: 1.09		***Chem. Eur. J. 2016, 22, 11196-11200
10.1002/chem.201602452
cyanide (in MeCN)
CN-*
 MeCN

N  Param.: 16.27

sN Param.: 0.70		***Angew. Chem. Int. Ed. 2005, 44, 142-145
10.1002/anie.200461640
cyano((diphenylmethylene)amino)methanide
*
 DMSO

N  Param.: 29.50

sN Param.: 0.50		*Tetrahedron 2019, 75, 459-463
10.1016/j.tet.2018.1[...]
cyano(pyridin-1-ium-1-yl)methanide (in DMSO)
C7H7N2*
 DMSO

N  Param.: 25.94

sN Param.: 0.42		***J. Am. Chem. Soc. 2013, 135, 15216-15224
10.1021/ja407885h
cyclohepta-1,3,5-trienyl-Fe(CO)3
*
 dichloromethane

N  Param.: 3.42

sN Param.: 0.94		***J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
cyclohepta-1,3-diene
C7H10*
 dichloromethane

N  Param.: 0.06

sN Param.: 1.10		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
cyclohexa-1,3-diene
C6H8*
 dichloromethane

N  Param.: 0.67

sN Param.: 1.10		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
cycloocta-1,3-diene
C8H12*
 dichloromethane

N  Param.: -0.50

sN Param.: 1.10		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
cyclopentadiene
C5H6*
 dichloromethane

N  Param.: 2.30

sN Param.: 1.06		***Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
cyclopentene
C5H8*
 dichloromethane

N  Param.: -1.55

sN Param.: 1.10		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
Danishefskys diene
C8H16O2Si*
 dichloromethane

N  Param.: 8.57

sN Param.: 0.84		*****J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
Desoxy Breslow intermediate 2a
*
 THF

N  Param.: 17.12

sN Param.: 0.80		***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
10.1002/anie.201202327
Desoxy Breslow intermediate 2a
*
 DMSO

N  Param.: 17.41

sN Param.: 0.74		***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
10.1002/anie.201202327
Desoxy Breslow intermediate 2a'
*
 THF

N  Param.: 14.45

sN Param.: 0.71		***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
10.1002/anie.201202327
Desoxy Breslow intermediate 2b
*
 THF

N  Param.: 13.91

sN Param.: 0.64		***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
10.1002/anie.201202327
Desoxy Breslow intermediate 2b'
*
 THF

N  Param.: 11.42

sN Param.: 0.70		***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
10.1002/anie.201202327
Desoxy Breslow intermediate 2c'
*
 THF

N  Param.: 12.75

sN Param.: 0.71		***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
10.1002/anie.201202327
Dexoxy Breslow intermediate 6
*
 THF

N  Param.: 15.58

sN Param.: 0.57		***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
10.1002/anie.201204524
diazoacetone
C3H4N2O*
 dichloromethane

N  Param.: 3.96

sN Param.: 0.91		***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
diazocyclopentadiene (in CH2Cl2)
C5H4N2*
 dichloromethane

N  Param.: 4.84

sN Param.: 1.06		***Synthesis 2023, 55, 354-358
10.1055/s-0041-1737327
diazomethane
CH2N2*
 dichloromethane

N  Param.: 10.48

sN Param.: 0.78		***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
diethyl diazomalonate
C7H10N2O4*
 dichloromethane

N  Param.: -0.35

sN Param.: 0.93		**Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
Dimedone iodonium ylide (in CH2Cl2)
*
 dichloromethane

N  Param.: 6.18

sN Param.: 0.81		***J. Am. Chem. Soc. 2016, 138, 10304-10313
10.1021/jacs.6b05768
Dimethyl 1,1'-isopropylidenezirconocene
*
 dichloromethane

N  Param.: 5.20

sN Param.: 1.00		*Chem. Eur. J. 2016, 22, 11196-11200
10.1002/chem.201602452
Dimethyl bis(indenyl)zirconium(IV)
*
 dichloromethane

N  Param.: 6.89

sN Param.: 1.00		*Chem. Eur. J. 2016, 22, 11196-11200
10.1002/chem.201602452
dimethyl diazomalonate
C5H6N2O4*
 dichloromethane

N  Param.: -1.24

sN Param.: 0.81		***J. Am. Chem. Soc. 2023, 145, 7416-7434
10.1021/jacs.2c13872
diphenyldiazomethane
C13H10N2*
 dichloromethane

N  Param.: 5.29

sN Param.: 0.92		***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
enolate of 2-coumaranone (in DMSO)
C8H5O2-*
 DMSO

N  Param.: 19.60

sN Param.: 0.75		***J. Org. Chem. 2024, 89, 6915-6928
10.1021/acs.joc.4c00277
enolate of 3-isochromanone (in DMSO)
C9H7O2-*
 DMSO

N  Param.: 25.39

sN Param.: 0.54		***J. Org. Chem. 2024, 89, 6915-6928
10.1021/acs.joc.4c00277
ethyl (E)-3-(dimethylamino)acrylate
C7H13NO2*
 dichloromethane

N  Param.: 9.43

sN Param.: 0.80		*Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
ethyl (E)-3-(N-morpholino)acrylate
C9H15NO3*
 dichloromethane

N  Param.: 8.52

sN Param.: 0.80		*Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
ethyl diazoacetate
C4H6N2O2*
 dichloromethane

N  Param.: 4.91

sN Param.: 0.95		***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
ethyl-vinylether
C4H8O*
 dichloromethane

N  Param.: 3.92

sN Param.: 0.90		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
fluorobis(phenylsulfonyl)methanide (in DMSO)
C13H10FO4S2*
 DMSO

N  Param.: 17.46

sN Param.: 0.73		***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
10.1002/anie.201605616
furan
C4H4O*
 dichloromethane

N  Param.: 1.33

sN Param.: 1.29		*****J. Am. Chem. Soc. 2012, 134, 13902-13911
10.1021/ja306522b
Indole
C8H7N*
 dichloromethane

N  Param.: 5.55

sN Param.: 1.09		***J. Org. Chem. 2006, 71, 9088-9095
10.1021/jo0614339
isobutylenyl-ethylether
C6H12O*
 dichloromethane

N  Param.: 4.23

sN Param.: 1.00		*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
lithium (5-methylfuran-2-yl)(4-(trifluoromethyl)phenyl)pinacolborate
C18H21BF3LiO3*
 MeCN

N  Param.: 8.13

sN Param.: 0.85		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)glycolborate
C15H12BF6LiO2S*
 MeCN

N  Param.: 11.23

sN Param.: 0.77		***Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)neopentylglycolborate
C18H18BF6LiO2S*
 MeCN

N  Param.: 10.13

sN Param.: 0.91		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)pinacolborate
C19H20BF6LiO2S*
 MeCN

N  Param.: 5.53

sN Param.: 1.00		*Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-(dimethylamino)phenyl)pinacolborate
C19H27BLiNO2S*
 MeCN

N  Param.: 8.02

sN Param.: 0.89		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)catecholglycolborate
C18H13BF3LiO2S*
 MeCN

N  Param.: 6.50

sN Param.: 0.77		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)neopentylglycolborate
C17H19BF3LiO2S*
 MeCN

N  Param.: 11.85

sN Param.: 0.72		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-chlorophenyl)pinacolborate
C17H21BClLiO2S*
 MeCN

N  Param.: 6.77

sN Param.: 0.88		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-methoxyphenyl)pinacolborate
C18H24BLiO3S*
 MeCN

N  Param.: 7.51

sN Param.: 0.87		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-methylphenyl)pinacolborate
C18H24BLiO2S*
 MeCN

N  Param.: 6.98

sN Param.: 0.93		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(phenyl)pinacolborate
C17H22BLiO2S*
 MeCN

N  Param.: 7.24

sN Param.: 0.83		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
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)
C18H22BF6LiO2*
 MeCN

N  Param.: 9.49

sN Param.: 0.82		***J. Am. Chem. Soc. 2017, 139, 15324-15327
10.1021/jacs.7b10240
lithium 2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C22H24BF6LiO2*
 MeCN

N  Param.: 7.46

sN Param.: 0.76		**Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 2-allyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)
C17H20BF6LiO2*
 MeCN

N  Param.: 8.71

sN Param.: 0.80		***J. Am. Chem. Soc. 2017, 139, 15324-15327
10.1021/jacs.7b10240
lithium 2-allyl-4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolan-2-uide (in MeCN)
C15H22BLiO2*
 MeCN

N  Param.: 11.20

sN Param.: 0.64		*J. Am. Chem. Soc. 2017, 139, 15324-15327
10.1021/jacs.7b10240
lithium 2-benzyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)
C21H22BF6LiO2*
 MeCN

N  Param.: 6.30

sN Param.: 0.78		**Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 2-benzyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C20H23BF3LiO2*
 MeCN

N  Param.: 7.15

sN Param.: 0.77		***Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 2-benzyl-4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolan-2-uide (in MeCN)
C19H24BLiO2*
 MeCN

N  Param.: 8.92

sN Param.: 0.70		**Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 2-cyclopropyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C16H21BF3LiO2*
 MeCN

N  Param.: 7.72

sN Param.: 0.75		*Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 2-ethyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C15H21BF3LiO2*
 MeCN

N  Param.: 7.68

sN Param.: 0.78		***Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 2-isopropyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C16H23BF3LiO2*
 MeCN

N  Param.: 6.63

sN Param.: 0.75		*Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 4,4,5,5-tetramethyl-2-(1-phenylethyl)-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C21H25BF3LiO2*
 MeCN

N  Param.: 8.56

sN Param.: 0.76		***Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 4,4,5,5-tetramethyl-2-phenyl-2-(1-phenylethyl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C20H26BLiO2*
 MeCN

N  Param.: 10.97

sN Param.: 0.63		**Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium 4,4,5,5-tetramethyl-2-phenyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolan-2-uide (in MeCN)
C15H22BLiO2*
 MeCN

N  Param.: 11.00

sN Param.: 0.57		***J. Am. Chem. Soc. 2022, 144, 16118-16130
10.1021/jacs.2c06493
lithium 5,5-dimethyl-2-(1-phenylethyl)-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborinan-2-uide (in MeCN)
C20H23BF3LiO2*
 MeCN

N  Param.: 11.29

sN Param.: 0.76		***Org. Lett. 2015, 17, 2614-2617
10.1021/acs.orglett.[...]
lithium bis(5-methylthiophen-2-yl)pinacolborate
C16H22BLiO2S2*
 MeCN

N  Param.: 7.67

sN Param.: 0.87		**Angew. Chem. Int. Ed. 2015, 54, 2780-2783
10.1002/anie.201410562
lithium indenide (in DMSO)
C9H7Li*
 DMSO

N  Param.: 23.66

sN Param.: 0.70		***Angew. Chem. Int. Ed. 2015, 54, 12497-12500
10.1002/anie.201501385
m-xylene
C8H10*
 dichloromethane

N  Param.: -3.57

sN Param.: 2.08		*****J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
Me2S(O)=CH2 (in DMSO)
*
 DMSO

N  Param.: 21.29

sN Param.: 0.47		***J. Am. Chem. Soc. 2010, 132, 17894-17900
10.1021/ja1084749
Me2S=CH(4-CN-C6H4) (in DMSO)
*
 DMSO

N  Param.: 21.07

sN Param.: 0.68		***J. Am. Chem. Soc. 2010, 132, 17894-17900
10.1021/ja1084749
Me2S=CH(p-NO2-C6H4) (in DMSO)
*
 DMSO

N  Param.: 18.42

sN Param.: 0.65		***J. Am. Chem. Soc. 2010, 132, 17894-17900
10.1021/ja1084749
Me2S=CH-CN (in DMSO)
*
 DMSO

N  Param.: 16.23

sN Param.: 0.60		***Chem. Eur. J. 2010, 16, 8610-8614
10.1002/chem.201001455
Me2S=CH-CO2Et (in DMSO)
*
 DMSO

N  Param.: 15.85

sN Param.: 0.61		***Chem. Eur. J. 2010, 16, 8610-8614
10.1002/chem.201001455
Meldrum's acid iodonium ylide (in CH2Cl2)
*
 dichloromethane

N  Param.: 4.36

sN Param.: 1.06		***J. Am. Chem. Soc. 2016, 138, 10304-10313
10.1021/jacs.6b05768
MeO-Breslow 1a
*
 THF

N  Param.: 14.77

sN Param.: 0.80		***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
10.1002/anie.201204524
MeO-Breslow 1b
*
 THF

N  Param.: 10.45

sN Param.: 0.81		***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
10.1002/anie.201204524
MeO-Breslow 1c
*
 THF

N  Param.: 16.61

sN Param.: 0.68		***Angew. Chem. Int. Ed. 2012, 51, 10408-10412
10.1002/anie.201204524