N-Nucleophiles

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Name	Solvent	Reactivity Parameters	Reference (title or year)
(S)-3-butyl-1-(pyrrolidin-2-ylmethyl)-1H-imidazol-3-ium trifluoromethanesulfonate	MeCN	N Param.: 13.57 s_N Param.: 0.53	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-4-benzyl-1,3-oxazolidin-2-one anion (in DMSO)	DMSO	N Param.: 22.67 s_N Param.: 0.54	J. Org. Chem. 2010, 75, 5250-5258 10.1021/jo1009883
(S)-4-phenyl-1-(pyrrolidin-2-ylmethyl)-1H-1,2,3-triazole	MeCN	N Param.: 15.32 s_N Param.: 0.72	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-5-benzyl-2,2,3-trimethylimidazolidin-4-one	MeCN	N Param.: 6.04 s_N Param.: 0.92	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-diphenyl(pyrrolidin-2-yl)methanol	MeCN	N Param.: 16.18 s_N Param.: 0.56	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-N,N-dimethyl-1-(pyrrolidin-2-yl)methanamine	MeCN	N Param.: 17.41 s_N Param.: 0.68	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-N,N-dimethylpyrrolidine-2-carboxamide	MeCN	N Param.: 17.61 s_N Param.: 0.67	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-N-propylpyrrolidine-2-carboxamide	MeCN	N Param.: 15.20 s_N Param.: 0.73	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-pyrrolidin-2-ylmethanamine	MeCN	N Param.: 17.24 s_N Param.: 0.67	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877
(S)-pyrrolidin-2-ylmethanol	MeCN	N Param.: 16.74 s_N Param.: 0.67	J. Am. Chem. Soc. 2020, 142, 1526-1547 10.1021/jacs.9b11877