Mayr's Database of Reactivity Parameters

C-Nucleophiles

3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 Found 562 molecules, displaying page 7 of 29 Results per page 10|50|100|all
Name Solvent Reactivity
Parameters
Classification Reference
(title or year)
diethyl diazomalonate
C7H10N2O4*
dichloromethane

N  Param.: -0.35

sN Param.: 0.93
**Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
diazomethane
CH2N2*
dichloromethane

N  Param.: 10.48

sN Param.: 0.78
***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
diazoacetone
C3H4N2O*
dichloromethane

N  Param.: 3.96

sN Param.: 0.91
***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
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
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
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 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 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 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
Danishefskys diene
C8H16O2Si*
dichloromethane

N  Param.: 8.57

sN Param.: 0.84
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
cyclopentene
C5H8*
dichloromethane

N  Param.: -1.55

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
cycloocta-1,3-diene
C8H12*
dichloromethane

N  Param.: -0.50

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
cyclohepta-1,3-diene
C7H10*
dichloromethane

N  Param.: 0.06

sN Param.: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
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
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
cyano((diphenylmethylene)amino)methanide
*
DMSO

N  Param.: 29.50

sN Param.: 0.50
*Tetrahedron 2019, 75, 459-463
10.1016/j.tet.2018.1[...]