Asymmetric synthesis of active pharmaceutical ingredients

被引:451
|
作者
Farina, Vittorio [1 ]
Reeves, Jonathan T. [1 ]
Senanayake, Chris H. [1 ]
Song, Jinhua J. [1 ]
机构
[1] Boehringer Ingelheim Pharmaceut Inc, Dept Chem Dev, Ridgefield, CT 06877 USA
关键词
D O I
10.1021/cr040700c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Over the years, a wide range of stereoselective synthetic methods have found applications in the large-scale asymmetric synthesis of active pharmaceutical ingredients (APIs). As a result, industrial process chemists have come to appreciate the value of these catalytic methods for the development of cost-effective, scalable, and environmentally sound processes, and have started to integrate these technologies into many API syntheses. In addition to a few well-established asymmetric catalytic protocols such as asymmetric hydrogenation and asymmetric epoxidation, many other types of catalytic transformations, such as asymmetric C-C bond-forming and dynamic kinetic resolution approaches, are slowly beginning to be incorporated into the large-scale synthesis of APIs.
引用
收藏
页码:2734 / 2793
页数:60
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