Chin. J. Org. Chem. ›› 2016, Vol. 36 ›› Issue (4): 752-759.DOI: 10.6023/cjoc201602032 Previous Articles     Next Articles



张松a, 陆俊筑a, 叶金星a, 段伟良b   

  1. a. 华东理工大学药学院 制药工程与过程化学研究中心 上海 200237;
    b. 中国科学院上海有机化学研究所 金属有机化学国家重点实验室 上海 200032
  • 收稿日期:2016-02-28 修回日期:2016-03-30 发布日期:2016-04-05
  • 通讯作者: 叶金星, 段伟良;
  • 基金资助:


Asymmetric C-H Arylation for the Synthesis of Planar Chiral Ferrocenes: Controlling Enantioselectivity Using Chiral Phosphoric Acids

Zhang Songa, Lu Junzhua, Ye Jinxinga, Duan Wei-liangb   

  1. a. School of Pharmacy, East China. University of Science and Technology, Shanghai 200237;
    b. State Key Laboratory of Organometallic. Chemistry, Shanghai Institute of Organic. Chemistry, Chinese Academy of Sciences, Shanghai 200032
  • Received:2016-02-28 Revised:2016-03-30 Published:2016-04-05
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Nos. 20902099, 21172238, 21472218).

Transition-metal-catalyzed direct activation reactions of unreactive C-H bond has been extensively developed in recent years. Although numerous synthetic methods have been reported to build diverse complex compounds, enantioselective C-H activation has not been paid much attention probably because of the absence of suitable ligands to control the stereoselectivity in the C-H activation reaction. Herein, a Pd(0)-catalyzed enantioselective synthesis of planar chiral ferrocenes was described, and chiral phosphoric acids were used as the only chiral source to control the stereoselectivity in the C-H activation reactions.

Key words: palladium catalysis, C-H activation, asymmetric catalysis, chiral phosphoric acids, ferrocenes