Chin. J. Org. Chem. ›› 2019, Vol. 39 ›› Issue (7): 1831-1836.DOI: 10.6023/cjoc201903001 Previous Articles     Next Articles



李秀英a, 李亚军b, 韦贤生a, 罗金荣a, 黄国保a, 谭明雄a   

  1. a 广西农产资源化学与生物技术重点实验室 玉林师范学院化学与食品科学学院 玉林 537000;
    b 湖南环境生物职业技术学院医药技术学院 衡阳 421005
  • 收稿日期:2019-03-01 修回日期:2019-03-30 发布日期:2019-04-16
  • 通讯作者: 黄国保, 谭明雄;
  • 基金资助:


Recent Progress on Reactions of Arylmethyl Azides with Alkenes

Li Xiuyinga, Li Yajunb, Wei Xianshenga, Luo Jinronga, Huang Guobaoa, Tan Minxionga   

  1. a Guangxi Key Laboratory of Agricultural Resources Chemistry and Biotechnology, College of Chemistry and Food Science of Yulin Normal University, Yulin 537000;
    b College of Medicine & Technology, Hunan Polytechnic of Environment and Biology, Hengyang 421005
  • Received:2019-03-01 Revised:2019-03-30 Published:2019-04-16
  • Contact: 10.6023/cjoc201903001;
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 21761033), the Natural Science Foundation of Guangxi (Nos. 2017GXNSFBA198211, 2018GXNSFAA294064), and the Yulin Normal University Research (Nos. 2018YJKY36, 201810606010).

Arylmethyl azides (ArCH2N3) as one of the significant nitrogen sources with stable properties, simple synthesis, have been widely used in a wide range of organic synthesis reactions. The recent progress (2014~2018) on reactions of arylmethyl azides with alkenes is summarized. In addition, the organic reactions of arylmethyl azides with types of alkenes are described respectively, with their scope of substrates and reaction mechanism. It is hoped that this review can be referred to the future application in organic synthesis of arylmethyl azides with alkenes.

Key words: arylmethyl azides, alkenes, reaction mechanism