Studies into the asymmetric Meisenheimer rearrangement

被引:12
作者
Buston, JEH
Coldham, I
Mulholland, KR
机构
[1] Univ Exeter, Dept Chem, Exeter EX4 4QD, Devon, England
[2] SmithKline Beecham Pharmaceut, Harlow CM19 5AW, Essex, England
关键词
D O I
10.1016/S0957-4166(98)00191-8
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Oxidation of a variety of N-allyl prolinol derivatives gave amine N-oxides with complete diastereoselectivity. On warming, these amine N-oxides undergo [2,3]-Meisenheimer rearrangement to give O-allyl hydroxylamines, albeit with low diastereoselectivity. Attempts to promote asymmetric N-oxidation of N-allyl tertiary amines with a variety of asymmetric oxidants produced only racemic N-oxides. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1995 / 2009
页数:15
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