C-Nucleophiles
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| Name | Solvent | Reactivity Parameters | Classification | Reference (title or year) | 
|---|---|---|---|---|
| anion of 1,2,3-triphenylpropane-1,3-dione (in DMSO)   | DMSO | N Param.: 14.99sN Param.: 0.83 |    | Eur. J. Org. Chem. 2017, , 1196-1202 10.1002/ejoc.201601513 | 
| barbiturate anion (in DMSO)   | DMSO | N Param.: 15.59sN Param.: 0.80 |    | J. Org. Chem. 2017, 82, 8476-8488 10.1021/acs.joc.7b01223 | 
| 1,3-dimethylbarbiturate anion (in DMSO)   | DMSO | N Param.: 17.46sN Param.: 0.72 |    | J. Org. Chem. 2017, 82, 8476-8488 10.1021/acs.joc.7b01223 | 
| 2-thiobarbiturate anion (in DMSO)   | DMSO | N Param.: 14.24sN Param.: 0.82 |    | J. Org. Chem. 2017, 82, 8476-8488 10.1021/acs.joc.7b01223 | 
| 1,3-diethyl-thiobarbiturate anion (in DMSO)   | DMSO | N Param.: 14.90sN Param.: 0.80 |    | J. Org. Chem. 2017, 82, 8476-8488 10.1021/acs.joc.7b01223 | 
| 4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane (in CH2Cl2)   | dichloromethane | N Param.: -0.64sN Param.: 1.10 |    | J. Am. Chem. Soc. 2017, 139, 15324-15327 10.1021/jacs.7b10240 | 
| lithium 2-allyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)   | MeCN | N Param.: 8.71sN Param.: 0.80 |    | J. Am. Chem. Soc. 2017, 139, 15324-15327 10.1021/jacs.7b10240 | 
| lithium (E)-2-(3,5-bis(trifluoromethyl)phenyl)-2-(but-2-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)   | MeCN | N Param.: 9.49sN Param.: 0.82 |    | J. Am. Chem. Soc. 2017, 139, 15324-15327 10.1021/jacs.7b10240 | 
| (E)-1-(2-(4-methoxyphenyl)-1-phenylvinyl)pyrrolidine (in MeCN)   | MeCN | N Param.: 11.99sN Param.: 0.84 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (E)-1-(1,2-diphenylvinyl)pyrrolidine (in MeCN)   | MeCN | N Param.: 11.66sN Param.: 0.82 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (E)-4-(2-phenyl-2-(pyrrolidin-1-yl)vinyl)benzonitrile (in MeCN)   | MeCN | N Param.: 10.63sN Param.: 0.84 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (E)-1-(2-(4-nitrophenyl)-1-phenylvinyl)pyrrolidine (in MeCN)   | MeCN | N Param.: 10.42sN Param.: 0.82 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (E)-1-(1,2-diphenylvinyl)piperidine (in MeCN)   | MeCN | N Param.: 9.94sN Param.: 0.86 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (E)-4-(1,2-diphenylvinyl)morpholine (in MeCN)   | MeCN | N Param.: 8.78sN Param.: 0.83 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (E)-beta-(N-piperidino)styrene (in MeCN)   | MeCN | N Param.: 13.84sN Param.: 0.73 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (E)-4-styrylmorpholine   | MeCN | N Param.: 11.66sN Param.: 0.83 |    | Chem. Eur. J. 2018, 24, 5901-5910 10.1002/chem.201705962 | 
| (p-nitrophenyl)diazomethane   | dichloromethane | N Param.: 7.17sN Param.: 0.83 |    | J. Am. Chem. Soc. 2018, 140, 16758-16772 10.1021/jacs.8b09995 | 
| (p-cyanophenyl)diazomethane   | dichloromethane | N Param.: 7.66sN Param.: 0.80 |    | J. Am. Chem. Soc. 2018, 140, 16758-16772 10.1021/jacs.8b09995 | 
| (p-bromophenyl)diazomethane   | dichloromethane | N Param.: 8.87sN Param.: 0.82 |    | J. Am. Chem. Soc. 2018, 140, 16758-16772 10.1021/jacs.8b09995 | 
| 1-(trimethylsiloxy)cyclopentene (in MeCN)   | MeCN | N Param.: 6.43sN Param.: 0.89 |    | Chem. Asian J. 2012, 7, 1401-1407 10.1002/asia.201101046 | 
