Chin. J. Org. Chem. ›› 2012, Vol. 32 ›› Issue (09): 1587-1604.DOI: 10.6023/cjoc201203009 Previous Articles     Next Articles



应安国, 武承林, 付永前, 任世斌, 梁华定   

  1. 台州学院医药化工学院 台州 318000
  • 收稿日期:2012-03-26 修回日期:2012-05-11 出版日期:2012-09-25 发布日期:2012-05-05
  • 通讯作者: 应安国
  • 基金资助:


Progress in the Application of Organocatalysis to Asymmetric Michael Additions

Ying Anguo, Wu Chenglin, Fu Yongqian, Ren Shibin, Liang Huading   

  1. School of Pharmaceutical and Chemical Engineering, Taizhou University, Taizhou 318000
  • Received:2012-03-26 Revised:2012-05-11 Online:2012-09-25 Published:2012-05-05
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No.21106090) and the Postdoctoral Foundation of China (No.2012M511352)

Organocatalysis has become one of the most intensively research fields. Asymmetric Michael addition is a key method for synthesis of versatile synthetic buildings and pharmaceutical intermediates, which include one or more stereo-chemical centers. The organocatalysts reported over the past three years for the asymmetric Michael addition are reviewed including primary amine, pyrrolidine based derivatives, (thio) urea, chiral squaramides and phosphoric acids. The relationship between structure of organocatalysts and their catalytic activities, catalytic reaction mechanism and the applications of these protocols for the preparation of drugs and bioactive intermediates are also introduced.

Key words: asymmetric Michael addition, organocatalysis, enantioselectivity, application