Conformational analysis of stereoselective epoxidations in flexible systems.

被引：2
|
作者：
Ducrot, P
Bucourt, R
Thal, C
机构：
[1] CNRS,INST CHIM SUBST NAT,F-91198 GIF SUR YVETTE,FRANCE
[2] FAC PHARM CHATENAY MALABRY,CNRS,URA 1843,LAB CHIM ORGAN,F-92296 CHATENAY MALABRY,FRANCE
来源：
TETRAHEDRON | 1996年 / 52卷 / 19期
关键词：
D O I：
10.1016/0040-4020(96)00320-1
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Approaching the transition state from both ends of the reaction pathway (the initial reactive conformation and the primary final form of the product), has enabled us to understand the unusually high stereoselectivity observed. Copyright (C) 1996 Elsevier Science Ltd
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页码：6699 / 6704
页数：6
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