Chinese Journal of Organic Chemistry ›› 2020, Vol. 40 ›› Issue (10): 3371-3379.DOI: 10.6023/cjoc202005064 Previous Articles     Next Articles


孙尚政c, 王星a,b, 程泰锦a,b, 徐辉a,b, 戴辉雄a,b   

  1. a 中国科学院上海药物研究所 上海 201203;
    b 中国科学院大学 北京 100049;
    c 上海大学化学系 上海大学创新药物研究中心 上海 200444
  • 收稿日期:2020-05-23 修回日期:2020-06-20 发布日期:2020-07-09
  • 通讯作者: 戴辉雄
  • 基金资助:

Cu(II)-Mediated β-C—H Alkynylation of Acrylamides with Terminal Alkynes

Sun Shangzhengc, Wang Xinga,b, Cheng Taijina,b, Xu Huia,b, Dai Huixionga,b   

  1. a Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203;
    b University of Chinese Academy of Sciences, Beijing 100049;
    c Department of Chemistry, Innovative Drug Research Center, Shanghai University, Shanghai 200444
  • Received:2020-05-23 Revised:2020-06-20 Published:2020-07-09
  • Supported by:
    Project supported by the National Natural Science Foundation of China (No. 21772211), the Youth Innovation Promotion Association CAS (Nos. 2014229, 2018293), and the Science and Technology Commission of Shanghai Municipality (No. 17JC1405000).

Cu(Ⅱ)-mediated b-C-H alkynylation of acrylamides with terminal alkynes is described by employing amide-oxazoline bidentate auxiliary, forming the conjugated 1,3-enynes. This protocol is characterized by its mild conditions, broad substarate scope and excellent regio- and stereo-selectivity.

Key words: b-C-H alkynylation, copper, 1,3-enynes, stereo-selectivity