Electrophiles
| Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
|---|---|---|---|---|
diphenylcarbodiimide   |
DMSO | E Param.: -20.14 |
 |
J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
carbon disulfide  |
DMSO | E Param.: -17.70 |
|
J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
3-methylcyclohexenone  |
DMSO | E Param.: -29.60 |
|
Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
3,6-dinitro-1-tosyl-1H-indole  |
E Param.: -12.90 |
|
Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j |
|
4-phenylbut-3-yn-2-one  |
E Param.: -16.90 |
 |
Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 |
|
hex-3-yn-2-one  |
E Param.: -17.90 |
|
Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 |
|
cycloheptenone  |
DMSO | E Param.: -22.00 |
|
Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
methyl diazoacetate  |
E Param.: -18.50 |
|
Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |
|
dimethyl diazomalonate  |
E Param.: -18.20 |
|
Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |
|
(p-nitrophenyl)diazomethane  |
E Param.: -18.30 |
|
Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |