Chinese Journal of Organic Chemistry ›› 2024, Vol. 44 ›› Issue (2): 335-348.DOI: 10.6023/cjoc202309006 Previous Articles     Next Articles



张剑a,b, 梁万洁c, 杨艺a, 闫法超a,*(), 刘会a,b,*()   

  1. a 山东理工大学化学化工学院 山东淄博 255049
    b 中国疾病预防控制中心环境与健康相关产品安全所 北京 100021
    c 山东安得医疗用品股份有限公司 淄博 255000
  • 收稿日期:2023-08-04 修回日期:2023-10-05 发布日期:2023-10-23
  • 基金资助:

Regiocontrollable Difunctionalization of N-Allenamines

Jian Zhanga,b, Wanjie Liangc, Yi Yanga, Fachao Yana(), Hui Liua,b()   

  1. a School of Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255049
    b China Center for Disease Control and Prevention Environmental and Health Related Product Safety Institute, Beijing 100021
    c Shandong Ande Healthcare Apparatus Co., Ltd., Zibo, Shandong 255000
  • Received:2023-08-04 Revised:2023-10-05 Published:2023-10-23
  • Contact:,
  • Supported by:
    National Natural Science Foundation of China(22078178)

As an electron-rich diene compound, N-allenamine has received wide spread attention in recent years due to its different reaction sites and high reactivity. Efficient and controllable regioselective functionalization of N-allenamines can successfully construct functionalized molecules. The research progress in the field of regioselective bifunctionalization of N-allenamines in recent years is mainly discussed, and the reaction mechanisms of most conversions in detail are discussed.

Key words: N-allenamine, regioselectivity, difunctionalization