Synthesis of both enantiomers of trans 3-hydroxypipecolic acid.

被引:51
作者
Greck, C
Ferreira, F
Genet, JP
机构
[1] Lab. de Synthèse Organique, Associé au CNRS, Ecl. Natl. Sup. de Chimie de Paris, 75231 Paris Cédex 05, 11, rue Pierre et Marie Curie
关键词
D O I
10.1016/0040-4039(96)00191-8
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The first syntheses of enantiomerically pure (2R, 3R) and (2S, 3S) 3-hydroxypipecolic acids 1 and 2 respectively, have been achieved from methyl 7-methyl-3-oxo-6-octenoate. Key steps involved asymmetric hydrogenation and electrophilic amination.
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页码:2031 / 2034
页数:4
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