Mayr's Database of Reactivity Parameters

Nucleophiles

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Name Solvent Reactivity
Parameters
Classification Reference
(title or year)
dibutylsulfide (in CH2Cl2)
C8H18S *
dichloromethane

N  Param.: 11.86

sN Param.: 0.74
** Chem. Eur. J. 2021, 21, 11367-11376
10.1002/chem.202100977
tetrahydrothiopyran (in CH2Cl2)
C5H10S *
dichloromethane

N  Param.: 11.94

sN Param.: 0.75
** Chem. Eur. J. 2021, 21, 11367-11376
10.1002/chem.202100977
3-methylanisole
C8H10O *
dichloromethane

N  Param.: 0.13

sN Param.: 1.27
*** J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
phenylacetylene
C8H6 *
dichloromethane

N  Param.: -0.04

sN Param.: 0.77
*** Angew. Chem. Int. Ed. 2014, 53, 4968-4971
10.1002/anie.201402055
phenylsilane
C6H8Si *
dichloromethane

N  Param.: 0.06

sN Param.: 0.71
*** Chem. Eur. J. 2013, 19, 249-263
10.1002/chem.201202839
triphenylsilane
C18H16Si *
dichloromethane

N  Param.: 2.65

sN Param.: 0.72
*** Chem. Eur. J. 2013, 19, 249-263
10.1002/chem.201202839
dimethyl(phenyl)silane
C8H12Si *
dichloromethane

N  Param.: 3.55

sN Param.: 0.75
*** Chem. Eur. J. 2013, 19, 249-263
10.1002/chem.201202839
triethylsilane
C6H16Si *
dichloromethane

N  Param.: 3.58

sN Param.: 0.70
*** J. Am. Chem. Soc. 2012, 134, 13902-13911
10.1021/ja306522b
triphenylgermane
C18H16Ge *
dichloromethane

N  Param.: 3.99

sN Param.: 0.62
*** J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
tributylsilane
C12H28Si *
dichloromethane

N  Param.: 3.99

sN Param.: 0.73
*** Chem. Eur. J. 2013, 19, 249-263
10.1002/chem.201202839
triphenylstannane
C18H16Sn *
dichloromethane

N  Param.: 5.64

sN Param.: 0.59
*** J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
tributylgermane
C12H28Ge *
dichloromethane

N  Param.: 5.92

sN Param.: 0.73
*** J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
borane-triethylamine-complex
C6H18BN *
dichloromethane

N  Param.: 8.90

sN Param.: 0.75
*** J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
tributylstannane
C12H28Sn *
dichloromethane

N  Param.: 9.96

sN Param.: 0.55
*** J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
1-(N-pyrrolidino)cyclopentene
C9H15N *
dichloromethane

N  Param.: 15.91

sN Param.: 0.86
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
1-(N-piperidino)cyclopentene
C10H17N *
dichloromethane

N  Param.: 15.06

sN Param.: 0.82
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
1-(N-pyrrolidino)cyclohexene
C10H17N *
dichloromethane

N  Param.: 14.91

sN Param.: 0.86
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
1-(N-morpholino)cyclopentene
C9H15NO *
dichloromethane

N  Param.: 13.41

sN Param.: 0.82
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
1-(phenylmethylamino)cyclopentene
C12H15N *
dichloromethane

N  Param.: 12.90

sN Param.: 0.79
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
1-(phenylmethylamino)cyclohexene
C13H17N *
dichloromethane

N  Param.: 10.73

sN Param.: 0.81
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
morpholinoisobutylene
C8H15NO *
dichloromethane

N  Param.: 10.04

sN Param.: 0.82
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
N-(triisopropylsilyl)pyrrole
C13H25NSi *
dichloromethane

N  Param.: 3.12

sN Param.: 0.93
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
Indole
C8H7N *
dichloromethane

N  Param.: 5.55

sN Param.: 1.09
*** J. Org. Chem. 2006, 71, 9088-9095
10.1021/jo0614339
N-methylindole
C9H9N *
dichloromethane

N  Param.: 5.75

sN Param.: 1.23
*** J. Org. Chem. 2006, 71, 9088-9095
10.1021/jo0614339
(E)-beta-(N-morpholino)styrene
C12H15NO *
dichloromethane

N  Param.: 10.76

sN Param.: 0.87
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
alpha-(N-morpholino)styrene
C12H15NO *
dichloromethane

N  Param.: 9.96

sN Param.: 0.79
*** Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
1,4-cyclohexadiene
C6H8 *
dichloromethane

N  Param.: 0.09

sN Param.: 0.98
*** J. Am. Chem. Soc. 2002, 124, 4076-4083
10.1021/ja0121538
1,4-dihydronaphthalene
C10H10 *
dichloromethane

N  Param.: -0.07

sN Param.: 1.03
*** J. Am. Chem. Soc. 2002, 124, 4076-4083
10.1021/ja0121538
9,10-dihydroanthracene
C14H12 *
dichloromethane

N  Param.: -0.86

sN Param.: 0.92
*** J. Am. Chem. Soc. 2002, 124, 4076-4083
10.1021/ja0121538
(E,E)-2,5-heptadiene
C7H12 *
dichloromethane

N  Param.: -0.74

sN Param.: 0.99
*** J. Am. Chem. Soc. 2002, 124, 4076-4083
10.1021/ja0121538
3-propylcyclopentene
C8H14 *
dichloromethane

N  Param.: -0.88

sN Param.: 0.94
*** J. Am. Chem. Soc. 2002, 124, 4076-4083
10.1021/ja0121538
H2O (in water)
H2O *
water

N  Param.: 5.20

sN Param.: 0.89
*** J. Am. Chem. Soc. 2004, 126, 5174-5181
10.1021/ja031828z
OH- (in 50/50 water/MeCN)
HO *
water-MeCN mix

N  Param.: 10.19

sN Param.: 0.62
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
OH- (in water)
HO *
water

N  Param.: 10.47

sN Param.: 0.61
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
semicarbazide (in water)
CH5N3O *
water

N  Param.: 11.05

sN Param.: 0.52
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
hydroxylamine (in water)
H3NO *
water

N  Param.: 11.41

sN Param.: 0.55
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
2,2,2-trifluoroethylamine (in DMSO)
C2H4F3N *
DMSO

N  Param.: 12.15

sN Param.: 0.65
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
2,2,2-trifluoroethanolate (in water)
C2H2F3O *
water

N  Param.: 12.66

sN Param.: 0.59
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
n-propylamine (in water)
C3H9N *
water

N  Param.: 13.33

sN Param.: 0.56
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
ethyl glycinate (in DMSO)
C4H9NO2 *
DMSO

N  Param.: 14.30

sN Param.: 0.67
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
HOO- (in water)
HO2 *
water

N  Param.: 15.40

sN Param.: 0.55
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
n-propylamine (in DMSO)
C3H9N *
DMSO

N  Param.: 15.70

sN Param.: 0.64
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
SO3(2-) (in water)
O3S *
water

N  Param.: 16.83

sN Param.: 0.56
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
morpholine (in DMSO)
C4H9NO *
DMSO

N  Param.: 16.96

sN Param.: 0.67
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
piperidine (in DMSO)
C5H11N *
DMSO

N  Param.: 17.19

sN Param.: 0.71
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
2-sulfidoacetate (in water)
C2H2O2S *
water

N  Param.: 22.62

sN Param.: 0.43
*** J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
anion of Meldrums acid (in DMSO)
C6H7O4 *
DMSO

N  Param.: 13.91

sN Param.: 0.86
*** Angew. Chem. Int. Ed. 2002, 41, 91-95
10.1002/1521-3773(20[...]
anion of dimedone (in DMSO)
C8H11O2 *
DMSO

N  Param.: 16.27

sN Param.: 0.77
*** Angew. Chem. Int. Ed. 2002, 41, 91-95
10.1002/1521-3773(20[...]
anion of acetylacetone (in DMSO)
C5H7O2 *
DMSO

N  Param.: 17.64

sN Param.: 0.73
*** Angew. Chem. Int. Ed. 2002, 41, 91-95
10.1002/1521-3773(20[...]
anion of ethyl acetylacetate (in DMSO)
C6H9O3 *
DMSO

N  Param.: 18.82

sN Param.: 0.69
*** Angew. Chem. Int. Ed. 2002, 41, 91-95
10.1002/1521-3773(20[...]