Stereoselective Michael additions of nitromethane yielding 3R(1S N-substituted aminoethyl)pyrrolidines
暂无分享，去创建一个
[1] S. Hagen,et al. Quinolone antibacterials containing the new 7-[3-(1-aminoethyl)-1- pyrrolidinyl] side chain: the effects of the 1-aminoethyl moiety and its stereochemical configurations on potency and in vivo efficacy. , 1993, Journal of medicinal chemistry.
[2] J. Domagala,et al. Synthesis of the four stereoisomers of several 3‐(1‐aminoethyl)pyrrolidines. Important intermediates in the preparation of quinolone antibacterials , 1992 .
[3] F. S. Guziec,et al. An improved method for the preparation of desoxopeffides—reductions of endothiopeptides☆ , 1990 .
[4] M. Reetz,et al. Stereoselective Synthesis of γ‐Aminocarboxylates , 1989 .
[5] B. Ganem,et al. Chemistry of naturally occurring polyamines. 10. Nonmetabolizable derivatives of spermine and spermidine , 1986 .
[6] W. C. Still,et al. Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination. , 1983 .