Dynamic kinetic resolutions and asymmetric transformations by enzymes coupled with metal catalysis

被引:174
作者
Kim, MJ [1 ]
Ahn, Y [1 ]
Park, J [1 ]
机构
[1] Pohang Univ Sci & Technol, Div Mol & Life Sci, Dept Chem, Natl Res Lab Chirotechnol, Pohang 790784, Kyungbuk, South Korea
关键词
D O I
10.1016/S0958-1669(02)00347-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The combination of enzyme and metal catalysis is described as a useful method for the synthesis of optically active compounds. A key feature of this new methodology is the use of metal catalysts for the in situ racemization of enzymatically unreactive enantiomers in the enzymatic resolution of racemic substrates. So far, two combinations - lipase-ruthenium and lipase-palladium - have been developed for the efficient dynamic kinetic resolution of alcohols and amines. The use of these combinations has also been extended to catalysis of the asymmetric transformation of ketones, their enol acetates, and ketoximes. In most cases, enzyme-metal combination catalysis has provided good yields and high optical purities.
引用
收藏
页码:578 / 587
页数:10
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