大学化学 >> 2025, Vol. 40 >> Issue (1): 196-205.doi: 10.12461/PKU.DXHX202404145

所属专题: 有机电化学

知识介绍 上一篇    下一篇

电化学烯烃氮杂环丙烷化的最新研究进展

何红1, 吴夏蝶1, 侯中伟1, 王磊1,2   

  1. 1 台州学院高等研究院和药学院, 浙江 台州 318000;
    2 杭州师范大学材料与化学化工学院, 有机硅化学及材料技术教育部重点实验室, 杭州 311121
  • 收稿日期:2024-04-25 录用日期:2024-05-29 发布日期:2025-01-06
  • 通讯作者: 侯中伟, 王磊 E-mail:zhongwei.hou@tzc.edu.cn;leiwang88@hotmail.com
  • 基金资助:
    国家自然科学基金(22071171,22101201)

Recent Advances in the Electrochemical Aziridination of Alkenes

Hong He1, Xiadie Wu1, Zhongwei Hou1, Lei Wang1,2   

  1. 1 Advanced Research Institute and School of Pharmaceutical Sciences, Taizhou University, Taizhou 318000, Zhejiang Province, China;
    2 Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, College of Material Chemistry, Chemical Engineering, Hangzhou Normal University, Hangzhou 311121, China
  • Received:2024-04-25 Accepted:2024-05-29 Published:2025-01-06
  • Contact: Zhongwei Hou, Lei Wang E-mail:zhongwei.hou@tzc.edu.cn;leiwang88@hotmail.com

摘要: 氮杂环丙烷是重要的有机结构骨架,可作为关键中间体构建结构多样的含氮化合物。有机电化学已经成为一种环境友好和可持续的有机合成工具,可以在不依赖外部氧化还原试剂的情况下实现各种化学转化。本文综述了电化学烯烃氮杂环丙烷化合成氮杂环丙烷的最新研究进展,重点介绍了这些转化的反应设计、活性中间体以及发展前景。

关键词: 电化学, 烯烃, 氮杂环丙烷化, 有机合成

Abstract: Aziridines are significant organic structural motifs that serve as key intermediates for the synthesis of diverse nitrogen-containing compounds. Organic electrochemistry has emerged as an environmentally friendly and sustainable approach to organic synthesis, facilitating a range of chemical transformations without the need for external redox reagents. This review highlights recent advancements in the electrochemical aziridination of alkenes for the synthesis of aziridines, with a focus on reaction design, active intermediates, and future prospects for development.

Key words: Electrochemistry, Alkenes, Aaziridination, Organic synthesis