Organocatalytic kinetic resolution of racemic primary alcohols using a chiral 1,2-diamine derived from (S)-proline
Organocatalytic kinetic resolution of racemic primary alcohols using a chiral 1,2-diamine derived from (S)-proline
复制标题
DOI：
10.1016/j.tetasy.2005.01.034
复制
发表时间：
2005-03-21
影响因子：
--
通讯作者：
Oriyama, T
中科院分区：
文献类型：
--
作者：
Terakado, D;Koutaka, H;Oriyama, T
由脯氨酸衍生的手性1，2-二胺催化外消旋伯醇与酰氯的不对称酰化反应，实现了高效率、高选择性的有机催化。(C)2005爱思唯尔有限公司保留所有权利。
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.