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合成α,β-二氨基酸衍生化合物的最有效途径。

Most efficient routes for the synthesis of alpha,beta-diamino acid-derived compounds.

机构信息

Center for Drug Discovery and Design, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, PR China.

出版信息

Curr Pharm Des. 2010;16(10):1252-9. doi: 10.2174/138161210790945968.

Abstract

Alpha,beta-Diamino acids have attracted considerable attention recently due to their growing importance in pharmaceutical and biochemical research. For example, this special class of alpha,beta-diamino acids has become the components of enzyme inhibitors, and has been incorporated into peptides which are used to modulate secondary and tertiary structural conformations. Although their widely occurrence in nature, optically active diamino acids are hard to isolate and purify from available natural resources on large scale. Therefore, their asymmetric synthesis becomes a great interest for organic and medicinal chemists. However, there still exist great challenges for enantioselective synthesis of diamino acids, especially those with two vicinal chiral centers. This review highlights the recent promising methodologies for enantioselective synthesis of alpha,beta-diamino acids, with special emphasis on catalytic asymmetric reactions, as well as methods for natural chiral compound derivatization, and chiral auxiliaries.

摘要

近年来,由于在药物和生化研究方面的重要性日益增加,α,β-二氨基酸受到了极大的关注。例如,这种特殊的α,β-二氨基酸类已成为酶抑制剂的组成部分,并已被整合到用于调节二级和三级结构构象的肽中。尽管它们在自然界中广泛存在,但光学活性的二氨基酸很难从现有自然资源中大规模分离和纯化。因此,它们的不对称合成成为有机和药物化学家的研究热点。然而,对于二氨基酸的对映选择性合成,特别是那些具有两个相邻手性中心的二氨基酸的对映选择性合成,仍然存在很大的挑战。本文综述了近年来α,β-二氨基酸对映选择性合成的最新有前途的方法,特别强调了催化不对称反应,以及天然手性化合物衍生化和手性助剂的方法。

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