Mayr's Database of Reactivity Parameters

N-Nucleophiles

For reactivities of structurally related compounds go to: Nucleophiles » N-Nucleophiles

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Name Solvent Reactivity
Parameters 		Classification Reference
(title or year)
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
phthalimide anion (in DMSO)
*
 DMSO

N  Param.: 15.52

sN Param.: 0.67		 *** 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
maleimide anion (in DMSO)
*
 DMSO

N  Param.: 14.87

sN Param.: 0.76		 *** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
trifluoroacetamide anion (in DMSO)
*
 DMSO

N  Param.: 15.81

sN Param.: 0.64		 *** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
N-methyl-trifluoroacetamide anion (in DMSO)
*
 DMSO

N  Param.: 15.70

sN Param.: 0.71		 *** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
4,4-dimethyl-glutarimide anion (in DMSO)
*
 DMSO

N  Param.: 17.52

sN Param.: 0.63		 *** 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
cyanamide anion (in DMSO)
*
 DMSO

N  Param.: 20.33

sN Param.: 0.64		 *** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
p-toluenesulfonamide anion (in DMSO)
*
 DMSO

N  Param.: 17.14

sN Param.: 0.60		 *** J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883