Chinese Journal of Organic Chemistry ›› 2022, Vol. 42 ›› Issue (1): 75-84.DOI: 10.6023/cjoc202107012 Previous Articles     Next Articles

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吲哚氮杂环作为自由基受体在串联环化反应中的研究进展

王弯弯a, 张明明b, 杨文超b,*(), 杨小虎c,*()   

  1. a 泰州学院医药与化学化工学院 江苏泰州 225300
    b 扬州大学园艺与植物保护学院 江苏扬州 225009
    c 浙江医院药剂科 杭州 310013
  • 收稿日期:2021-07-05 修回日期:2021-09-01 发布日期:2021-09-08
  • 通讯作者: 杨文超, 杨小虎
  • 基金资助:
    江苏省高校自然科学基金(19KJB150020)

Research Progress in Radical Cascade Reaction Using Nitrogen Heterocycle in Indoles as Radical Acceptors

Wanwan Wanga, Mingming Zhangb, Wenchao Yangb(), Xiaohu Yangc()   

  1. a College of Pharmacy and Chemistry & Chemical Engineering, Taizhou University, Taizhou, Jiangsu 225300
    b School of Horticulture and Plant Protection, Yangzhou University, Yangzhou, Jiangsu 225009
    c Department of Pharmacy, Zhejiang Hospital, Hangzhou 310013
  • Received:2021-07-05 Revised:2021-09-01 Published:2021-09-08
  • Contact: Wenchao Yang, Xiaohu Yang
  • Supported by:
    Natural Science Foundation of the Jiangsu Higher Education Institutions of China(19KJB150020)

Indole skeleton has been widely utilized in the synthesis and late-stage modification of biologically active compounds, especially in the fields of medicines and pesticides. In recent years, constructing spiro compounds by asymmetric dearomatization of indoles has become extremely promising. Meanwhile, the radical tandem reaction of unsaturated bonds has been a significant branch of organic chemistry, and this methodology has become a crucial approach to modify the indole skeleton. Therefore, the recent progress in the field of radical cascade reaction of unsaturated hydrocarbon using nitrogen heterocycle in indoles as radical acceptors is summarized. Besides, the reaction design, mechanism and prospects of this field are also discussed.

Key words: indole, radical, cascade cyclization reactions, unsaturated bonds, difunctionalization