Mayr's Database of Reactivity Parameters

C-Nucleophiles

19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 Found 572 molecules, displaying page 23 of 29 Results per page 10|50|100|all
Name Solvent Reactivity
Parameters
Classification Reference
(title or year)
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 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 2c'
*
THF

N  Param.: 12.75

sN Param.: 0.71
***Angew. Chem. Int. Ed. 2012, 51, 6231-6235
10.1002/anie.201202327
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
diazoacetone
C3H4N2O*
dichloromethane

N  Param.: 3.96

sN Param.: 0.91
***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
diazomethane
CH2N2*
dichloromethane

N  Param.: 10.48

sN Param.: 0.78
***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
diethyl diazomalonate
C7H10N2O4*
dichloromethane

N  Param.: -0.35

sN Param.: 0.93
**Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
Dimedone iodonium ylide (in CH2Cl2)
*
dichloromethane

N  Param.: 6.18

sN Param.: 0.81
***J. Am. Chem. Soc. 2016, 138, 10304-10313
10.1021/jacs.6b05768
Dimethyl 1,1'-isopropylidenezirconocene
*
dichloromethane

N  Param.: 5.20

sN Param.: 1.00
*Chem. Eur. J. 2016, 22, 11196-11200
10.1002/chem.201602452
Dimethyl bis(indenyl)zirconium(IV)
*
dichloromethane

N  Param.: 6.89

sN Param.: 1.00
*Chem. Eur. J. 2016, 22, 11196-11200
10.1002/chem.201602452
dimethyl diazomalonate
C5H6N2O4*
dichloromethane

N  Param.: -1.24

sN Param.: 0.81
***J. Am. Chem. Soc. 2023, 145, 7416-7434
10.1021/jacs.2c13872
diphenyldiazomethane
C13H10N2*
dichloromethane

N  Param.: 5.29

sN Param.: 0.92
***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
enolate of 2-coumaranone (in DMSO)
C8H5O2-*
DMSO

N  Param.: 19.60

sN Param.: 0.75
***J. Org. Chem. 2024, 89, 6915-6928
10.1021/acs.joc.4c00277
enolate of 3-isochromanone (in DMSO)
C9H7O2-*
DMSO

N  Param.: 25.39

sN Param.: 0.54
***J. Org. Chem. 2024, 89, 6915-6928
10.1021/acs.joc.4c00277
ethyl (E)-3-(dimethylamino)acrylate
C7H13NO2*
dichloromethane

N  Param.: 9.43

sN Param.: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
ethyl (E)-3-(N-morpholino)acrylate
C9H15NO3*
dichloromethane

N  Param.: 8.52

sN Param.: 0.80
*Chem. Eur. J. 2003, 9, 2209-2218
10.1002/chem.200204666
ethyl diazoacetate
C4H6N2O2*
dichloromethane

N  Param.: 4.91

sN Param.: 0.95
***Chem. Eur. J. 2003, 9, 4068-4076
10.1002/chem.200304913
ethyl-vinylether
C4H8O*
dichloromethane

N  Param.: 3.92

sN Param.: 0.90
*Acc. Chem. Res. 2003, 36, 66-77
10.1021/ar020094c
fluorobis(phenylsulfonyl)methanide (in DMSO)
C13H10FO4S2*
DMSO

N  Param.: 17.46

sN Param.: 0.73
***Angew. Chem. Int. Ed. 2016, 55, 12845-12848
10.1002/anie.201605616