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腈酶催化的α-硫代腈动态动力学拆分对映选择性合成α-硫代羧酸。

Enantioselective Synthesis of α-Thiocarboxylic Acids by Nitrilase Biocatalysed Dynamic Kinetic Resolution of α-Thionitriles.

机构信息

School of Cancer and Pharmaceutical Sciences, King's College London, 150 Stamford Street, SE1 9NH, London, UK.

Prozomix Limited, West End Industrial Estate, Haltwhistle, Northumberland, NE49 9HA, UK.

出版信息

Chemistry. 2020 Aug 17;26(46):10422-10426. doi: 10.1002/chem.202001108. Epub 2020 Jul 16.

Abstract

The enantioselective synthesis of α-thiocarboxylic acids by biocatalytic dynamic kinetic resolution (DKR) of nitrile precursors exploiting nitrilase enzymes is described. A panel of 35 nitrilase biocatalysts were screened and enzymes Nit27 and Nit34 were found to catalyse the DKR of racemic α-thionitriles under mild conditions, affording the corresponding carboxylic acids with high conversions and good-to-excellent ee. The ammonia produced in situ during the biocatalytic transformation favours the racemization of the nitrile enantiomers and, in turn, the DKR without the need of any external additive base.

摘要

利用腈水解酶对腈前体进行生物催化动态动力学拆分(DKR)实现α-硫代羧酸的对映选择性合成。本文筛选了 35 种腈水解酶生物催化剂,发现酶 Nit27 和 Nit34 在温和条件下能够催化外消旋α-硫代腈的 DKR,以高转化率和良好至优秀的对映体过量值(ee)得到相应的羧酸。生物催化转化过程中原位生成的氨有利于腈对映异构体的外消旋化,从而无需任何外加碱添加剂即可进行 DKR。

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