DIASTEREOFACIAL SELECTIVITY IN THE 1,3-DIPOLAR CYCLOADDITION OF CHIRAL AZOMETHINE YLIDES

被引：21
|
作者：
DEPREZ, P [1 ]
ROUDEN, J [1 ]
CHIARONI, A [1 ]
RICHE, C [1 ]
ROYER, J [1 ]
HUSSON, HP [1 ]
机构：
[1] CNRS,INST CHIM SUBST NAT,F-91198 GIF SUR YVETTE,FRANCE
来源：
TETRAHEDRON LETTERS | 1991年 / 32卷 / 51期
关键词：
D O I：
10.1016/0040-4039(91)80526-C
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Diastereofacial stereoselectivity in the cycloaddition of azomethine ylides obtained from N-methoxycarbonylmethyloxazolidine 4 with N-phenylmaleimide is studied relative to R1 and R2 groups borne by the chiral auxiliary moiety.
引用
收藏
页码：7531 / 7534
页数：4
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