Diastereoselective and regioselective singlet-oxygen ene reaction of oxazolidine-substituted alkenes: Control through hydrogen bonding mediated by the urea functionality of chiral auxiliaries

被引：30

作者：

Adam, W

Peters, K

Peters, EM

Schambony, SB ^{[1
]}

机构：

[1] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany

[2] Max Planck Inst Festkorperforsch, D-70569 Stuttgart, Germany

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2000年 / 122卷 / 31期

关键词：

D O I：

10.1021/ja001113l

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：7610 / 7611

页数：2

共 32 条

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[8] Adam W, 1998, EUR J ORG CHEM, V1998, P501
[9] Diastereoselective singlet oxygen ene reaction (Schenck reaction) and diastereoselective epoxidations of heteroatom-substituted acyclic chiral olefins: A mechanistic comparison
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[10] Hydroxy group directivity in the epoxidation of chiral allylic alcohols: Control of diastereoselectivity through allylic strain and hydrogen bonding
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[J]. ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (08) : 703 - 710

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