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伯氨基酸:对映选择性有机催化中的优势催化剂。

Primary amino acids: privileged catalysts in enantioselective organocatalysis.

作者信息

Xu Li-Wen, Lu Yixin

机构信息

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Republic of Singapore.

出版信息

Org Biomol Chem. 2008 Jun 21;6(12):2047-53. doi: 10.1039/b803116a. Epub 2008 Apr 21.

Abstract

Despite the recent spectacular advances in asymmetric organocatalysis, proline and its analogues have been predominantly employed as organocatalysts in reactions utilizing enamine intermediates. Recent studies of enantioselective organocatalytic reactions promoted by primary amino acids and their derivatives are described in this account. The primary amino functions, rather than the secondary pyrrolidine moiety, have been shown to provide unique reactivity and stereoselectivity in asymmetric aldol and Mannich reactions.

摘要

尽管最近不对称有机催化取得了惊人进展,但脯氨酸及其类似物在利用烯胺中间体的反应中一直主要用作有机催化剂。本文介绍了由伯氨基酸及其衍生物促进的对映选择性有机催化反应的最新研究。结果表明,在不对称羟醛反应和曼尼希反应中,起独特反应性和立体选择性作用的是伯氨基官能团,而非仲吡咯烷部分。

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