Mayr's Database of Reactivity Parameters

N-Nucleophiles

1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 Found 342 molecules, displaying page 4 of 18 Results per page 10|50|100|all
Name Solvent Reactivity
Parameters
Classification Reference
(title or year)
O-DHPB (in CH2Cl2)
C10H10N2O*
dichloromethane

N  Param.: 13.31

sN Param.: 0.69
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
O-HyperBTM (in CH2Cl2)
C19H20N2O*
dichloromethane

N  Param.: 13.01

sN Param.: 0.73
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
Te-BTM (in CH2Cl2)
C15H12N2Te*
dichloromethane

N  Param.: 14.62

sN Param.: 0.66
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
Se-DHPB (in CH2Cl2)
C10H10N2Se*
dichloromethane

N  Param.: 15.16

sN Param.: 0.66
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
Se-tetramisole (Se-TM) (in CH2Cl2)
C11H12N2Se*
dichloromethane

N  Param.: 15.26

sN Param.: 0.60
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
Se-BTM (in CH2Cl2)
C15H12N2Se*
dichloromethane

N  Param.: 14.27

sN Param.: 0.63
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
Se-HBTM (in CH2Cl2)
C16H14N2Se*
dichloromethane

N  Param.: 14.42

sN Param.: 0.67
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
Se-HyperBTM (in DCM)
C19H20N2Se*
dichloromethane

N  Param.: 16.11

sN Param.: 0.58
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
Te-DHPB (in CH2Cl2)
C10H10N2Te*
dichloromethane

N  Param.: 16.63

sN Param.: 0.65
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
tetramisole (TM) (in CH2Cl2)
C11H12N2S*
dichloromethane

N  Param.: 13.86

sN Param.: 0.68
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
BTM (in CH2Cl2)
C15H12N2S*
dichloromethane

N  Param.: 13.06

sN Param.: 0.73
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
7-F-BTM (in CH2Cl2)
C15H11FN2S*
dichloromethane

N  Param.: 13.46

sN Param.: 0.66
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
7-MeO-BTM (in CH2Cl29
C16H14N2OS*
dichloromethane

N  Param.: 13.15

sN Param.: 0.75
***Angew. Chem. Int. Ed. 2025, EarlyView, e202514865
10.1002/anie.202514865
4-(dimethylamino)pyridine (in DMF)
C7H10N2*
DMF

N  Param.: 14.90

sN Param.: 0.67
*Chem. Eur. J. 2007, 13, 336-345
10.1002/chem.200600941
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
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
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
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
azide ion (in DMSO)
N3-*
DMSO

N  Param.: 20.50

sN Param.: 0.59
***J. Phys. Org. Chem. 2006, 19, 706-713
10.1002/poc.1063