Mayr's Database of Reactivity Parameters

N-Nucleophiles

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Name Solvent Reactivity
Parameters
Classification Reference
(title or year)
7-PivO-HyperBTM
C24H28N2O2S *
dichloromethane

N  Param.: 14.49

sN Param.: 0.66
*** ChemistryEurope 2026, 4, e202500434
10.1002/ceur.202500434
7-Ms-HyperBTM
C20H22N2O2S2 *
dichloromethane

N  Param.: 12.52

sN Param.: 0.75
*** ChemistryEurope 2026, 4, e202500434
10.1002/ceur.202500434
HyperNTM
C23H22N2S *
dichloromethane

N  Param.: 14.47

sN Param.: 0.72
*** ChemistryEurope 2026, 4, e202500434
10.1002/ceur.202500434
HyperPTM
C27H24N2S *
dichloromethane

N  Param.: 13.43

sN Param.: 0.79
*** ChemistryEurope 2026, 4, e202500434
10.1002/ceur.202500434
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