Chin. J. Org. Chem. ›› 2019, Vol. 39 ›› Issue (9): 2365-2378.DOI: 10.6023/cjoc201903041 Previous Articles     Next Articles



刘奕奕a, 周荣b   

  1. a 国网湖南省电力有限公司电力科学研究院 长沙 410007;
    b 太原理工大学化学化工学院 太原 030024
  • 收稿日期:2019-03-21 修回日期:2019-04-20 发布日期:2019-05-06
  • 通讯作者: 刘奕奕, 周荣;
  • 基金资助:


Progress in Annulation Reactions Based on Huisgen Zwitterion

Liu Yiyia, Zhou Rongb   

  1. a State Grid Hunan Electric Power Corporation Limited Research Institute, Changsha 410007;
    b College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024
  • Received:2019-03-21 Revised:2019-04-20 Published:2019-05-06
  • Contact: 10.6023/cjoc201903041;
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 21502135), the Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi Province (No. 201802024).

The development of highly efficient and selective synthetic methodologies is an important research task in organic chemistry. In recent years, the Huisgen zwitterions, a type of intermediates derived from nucleophilic addition of tertiary phosphine to azodicarboxylates, have shown unique superiority and efficiency in synthesis of azacyclic compounds, and therefore have attracted broad interest from organic chemists. A large number of annulation reactions based on Huisgen zwitterions have been reported. According to the types of electrophiles, the annulation reactions of Husigen zwitterions with carbonyl compounds, electron-deficient alkenes, imines, and other electrophiles are summarized, respectively.

Key words: Huisgen zwitterion, tertiary phosphine, azodicarboxylate, azacyclic compounds, annulation reaction