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手性氨基酸的酶法不对称合成。

Enzymatic asymmetric synthesis of chiral amino acids.

机构信息

Key Laboratory of Bioorganic Synthesis of Zhejiang Province, College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310014, China.

出版信息

Chem Soc Rev. 2018 Feb 19;47(4):1516-1561. doi: 10.1039/c7cs00253j.

Abstract

Chiral amino acids are extensively applied in the pharmaceutical, food, cosmetic, agricultural, and feedstuff industries. The development of synthetic methodologies for optically pure amino acids has been driven by their significant applications. Among the various synthesis methods for the production of chiral amino acids, enzymatic asymmetric synthesis is a unique preparation strategy that shows great potential. This review provides an overview of the reported methods for enzymatic asymmetric synthesis of chiral amino acids, including asymmetric reductive amination of keto acids, asymmetric transfer of an amino group to keto acids, enantioselective addition of ammonia to α,β-unsaturated acids, and aldol condensation of an amino acid to aldehydes.

摘要

手性氨基酸在医药、食品、化妆品、农业和饲料等行业得到了广泛应用。由于其重要的应用价值,光学纯氨基酸的合成方法得到了极大的发展。在生产手性氨基酸的各种合成方法中,酶法不对称合成是一种独特的制备策略,具有很大的潜力。本文综述了近年来报道的酶法不对称合成手性氨基酸的方法,包括酮酸的不对称还原胺化、酮酸的氨基不对称转移、氨对α,β-不饱和酸的对映选择性加成以及氨基酸与醛的醛醇缩合。

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