N-Nucleophiles
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| Name | Solvent | Reactivity Parameters | Classification | Reference (title or year) | 
|---|---|---|---|---|
| (S)-2-(diphenyl((trimethylsilyl)oxy)methyl)pyrrolidine   | MeCN | N Param.: 12.03sN Param.: 0.98 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| (S)-diphenyl(pyrrolidin-2-yl)methanol   | MeCN | N Param.: 16.18sN Param.: 0.56 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| (S)-2-(azidodiphenylmethyl)pyrrolidine   | MeCN | N Param.: 9.90sN Param.: 1.22 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| 2-(triphenylsilyl)pyrrolidine   | MeCN | N Param.: 14.00sN Param.: 0.84 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| (S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one   | MeCN | N Param.: 6.04sN Param.: 0.92 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| (2S,5S)-5-benzyl-2-(tert-butyl)-3-methylimidazolidin-4-one   | MeCN | N Param.: 5.44sN Param.: 1.12 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| (2S,5S)-5-benzyl-3-methyl-2-(5-methylfuran-2-yl)imidazolidin-4-one   | MeCN | N Param.: 8.76sN Param.: 0.89 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| (2R,5S)-5-benzyl-3-methyl-2-(5-methylfuran-2-yl)imidazolidin-4-one   | MeCN | N Param.: 7.39sN Param.: 1.00 |    | J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877 | 
| TCAP (in MeCN)   | MeCN | N Param.: 15.60sN Param.: 0.68 |    | Chem. Eur. J. 2013, 19, 6435-6442 10.1002/chem.201204452 | 
| 4-pyrrolidinopyridine (in MeCN)   | MeCN | N Param.: 14.99sN Param.: 0.69 |    | Chem. Eur. J. 2013, 19, 6435-6442 10.1002/chem.201204452 | 
| (S)-3,3-difluoro-2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine (in CH2Cl2)   | dichloromethane | N Param.: 10.83sN Param.: 0.80 |    | ARKIVOC 2024, (4), 202312093 10.24820/ark.5550190[...] | 
| pyridine (in MeCN)   | MeCN | N Param.: 13.60sN Param.: 0.60 |    | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 | 
| 2-methylpyridine (in CH2Cl2)   | dichloromethane | N Param.: 10.52sN Param.: 0.78 |    | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 | 
| 2-methylpyridine (in MeCN)   | MeCN | N Param.: 10.98sN Param.: 0.66 |    | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 | 
| 2,6-dimethylpyridine (in CH2Cl2)   | dichloromethane | N Param.: 9.87sN Param.: 0.68 |    | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 | 
| 2,6-dimethylpyridine (in MeCN)   | MeCN | N Param.: 9.11sN Param.: 0.69 |    | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 | 
| 2,4,6-trimethylpyridine (in CH2Cl2)   | dichloromethane | N Param.: 9.34sN Param.: 0.71 |    | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 | 
| 2,4,6-trimethylpyridine (in MeCN)   | MeCN | N Param.: 9.39sN Param.: 0.60 |    | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 | 
| pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Ph4P+) (in CH2Cl2)   | dichloromethane | N Param.: 17.88sN Param.: 0.73 |    | J. Am. Chem. Soc. 2025, 147, 5043-5050 10.1021/jacs.4c14825 | 
| ((4-methoxyphenyl)sulfonyl)(pyridin-4-yl)amide (Ph4P+) (in CH2Cl2)   | dichloromethane | N Param.: 19.63sN Param.: 0.65 |    | J. Am. Chem. Soc. 2025, 147, 5043-5050 10.1021/jacs.4c14825 | 
