化学
还原胺化
胺化
立体选择性
胺气处理
生物催化
溶剂
肺表面活性物质
有机化学
组合化学
溶剂极性
离子键合
绿色化学
离子液体
化学工程
催化作用
生物化学
离子
工程类
作者
Andrea Fiorati,Per Berglund,Maria Svedendahl Humble,Davide Tessaro
标识
DOI:10.1002/adsc.201901434
摘要
Abstract The challenging bioamination of hydrophobic substrates has been attained through the employment of a disperse system consisting of a combination of a low polarity solvent (e. g. isooctane or methyl‐ tert ‐butylether), a non‐ionic surfactant and a minimal amount of water. In these conditions, amine transaminases (ATA) were shown to efficiently carry out the reductive amination of variously substituted cyclohexanones, providing good conversions often coupled with a superior stereoselectivity if compared with the corresponding chemical reductive amination. An array of synthetically useful 4‐substituted aminocyclohexanes was consequentially synthesized through biocatalysis, analyzed and stereochemically characterized. magnified image
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