Chin. J. Org. Chem. ›› 2019, Vol. 39 ›› Issue (1): 249-256.DOI: 10.6023/cjoc201807013 Previous Articles     Next Articles



张娟, 王碧云, 刘熠森, 曹松   

  1. 上海市化学生物学(芳香杂环)重点实验室 华东理工大学药学院 上海 200237
  • 收稿日期:2018-07-06 修回日期:2018-09-05 发布日期:2018-09-18
  • 通讯作者: 曹松
  • 基金资助:


Stereoselective Synthesis of Z-Fluorostyrene Derivatives via Nickel-Catalyzed Cross-Coupling of gem-Difluorostyrenes with Organozinc Reagents

Zhang Juan, Wang Biyun, Liu Yisen, Cao Song   

  1. Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology(ECUST), Shanghai 200237
  • Received:2018-07-06 Revised:2018-09-05 Published:2018-09-18
  • Contact: 10.6023/cjoc201807013
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Nos. 21472043, 21272070).

An efficient method for the synthesis of various Z-fluorostyrene derivatives via nickel-catalyzed cross-coupling of gem-difluorostyrenes with organozinc reagents with the assistance of LiCl was developed. The reaction proceeds efficiently under mild condition, affording monofluoroalkenes in moderate to good yields. This novel method exhibits good functional group compatibility and excellent stereoselectivity.

Key words: gem-difluorostyrenes, nickel-catalyzed, organozinc reagents, monofluoroalkenes