Enantioselective C-C bond synthesis catalysed by enzymes

被引:120
|
作者
Sukumaran, J [1 ]
Hanefeld, U [1 ]
机构
[1] Tech Univ Delft, NL-2628 BL Delft, Netherlands
关键词
D O I
10.1039/b412490a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The enantioselective synthesis of C-C bonds is often the pivotal step of a synthesis. Nature has made a variety of versatile enzymes available that catalyse this type of reaction very selectively under mild conditions. Cyanohydrins, acyloins (alpha-hydroxy ketones), alpha-hydroxy acids and aldols (beta-hydroxy ketones) are very efficiently synthesised enantioselectively with the aid of C-C bond forming enzymes, which we discuss in this tutorial review. In the case of the alpha-hydroxy acids the applications of nitrilases in a synthetic dkr even allows a disconnection that has no enantioselective chemical equivalent.
引用
收藏
页码:530 / 542
页数:13
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