Organocatalytic kinetic resolution of racemic primary alcohols using a chiral 1,2-diamine derived from (S)-proline

被引：47

作者：

Terakado, D ^{[1
]}

Koutaka, H ^{[1
]}

Oriyama, T ^{[1
]}

机构：

[1] Ibaraki Univ, Fac Sci, Ibaraki 3108512, Japan

来源：

TETRAHEDRON-ASYMMETRY | 2005年 / 16卷 / 06期

关键词：

D O I：

10.1016/j.tetasy.2005.01.034

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A highly efficient and good enantioselective organocatalytic asymmetric acylation of racemic primary alcohols with acyl chlorides has been achieved catalyzed by a chiral 1,2-diamine derived from (S)-proline. (C) 2005 Elsevier Ltd. All rights reserved.

引用

页码：1157 / 1165

页数：9

共 47 条

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