亚胺
还原胺化
化学
组合化学
生物催化
胺化
有机化学
催化作用
反应机理
作者
Gheorghe‐Doru Roiban,Marcelo Kern,Zhi Liu,Julia F. Hyslop,Pei Lyn Tey,Matthew S. Levine,Lydia S. Jordan,Kristin K. Brown,Timin Hadi,Leigh Anne F. Ihnken,Murray J. B. Brown
出处
期刊:Chemcatchem
[Wiley]
日期:2017-08-28
卷期号:9 (24): 4475-4479
被引量:94
标识
DOI:10.1002/cctc.201701379
摘要
Abstract Chiral secondary and tertiary amines are ubiquitous in pharmaceutical, fine, and specialty chemicals, but their synthesis typically suffers from significant sustainability and selectivity challenges. Biocatalytic alternatives, such as enzyme‐catalyzed reductive amination, offer several advantages over traditional chemistry, but industrial applicability has not yet been demonstrated. Herein, we report the use of cell lysates expressing imine reductases operating at 1:1 stoichiometry for a variety of amines and carbonyls. A collection of biocatalysts with diversity in coverage of small molecules and direct industrial applicability is presented.
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