Chin. J. Org. Chem. ›› 2017, Vol. 37 ›› Issue (3): 566-576.DOI: 10.6023/cjoc201610011 Previous Articles     Next Articles



袁斯甜a, 王艳华a, 邱观音生b, 刘晋彪a   

  1. a 江西理工大学冶金与化学工程学院 赣州 341000;
    b 嘉兴学院生物与化学工程学院 嘉兴 314001
  • 收稿日期:2016-10-09 修回日期:2016-11-11 发布日期:2016-11-22
  • 通讯作者: 刘晋彪,;邱观音生,;
  • 基金资助:


Recent Advances in Radical Initiated C-N Bond Formation under Transition Metal-Free Conditions

Yuan Sitiana, Wang Yanhuaa, Qiu Guanyinshengb, Liu Jinbiaoa   

  1. a School of Metallurgical and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000;
    b College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing 314001
  • Received:2016-10-09 Revised:2016-11-11 Published:2016-11-22
  • Contact: 10.6023/cjoc201610011;
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Nos. 21502075, 21502069) and the Natural Science Foundation of Zhejiang Province (No. LQ15B020006).

Nitrogen-containing compounds are extremely important because of their abundance in synthetic organic compounds, natural products and pharmaceutical agents. Recently, transition metal-free C-N bond-formation via radical procedures has attracted wide interest. The recent advances in C-N bond formation via C(sp3, sp2 or sp)-H bond activation under transition metal-free conditions are summarized.

Key words: C-H activation, C-N bond, radical, dehydrogenative coupling