Chin. J. Org. Chem. ›› 2015, Vol. 35 ›› Issue (3): 588-602.DOI: 10.6023/cjoc201411035 Previous Articles     Next Articles



王浩a, 许斌a,b,c   

  1. a 上海大学化学系 上海 200444;
    b 中国科学院上海有机化学研究所 金属有机化学国家重点实验室 上海 200032;
    c 华东师范大学 上海市绿色化学与化工过程绿色化重点实验室 上海 200062
  • 收稿日期:2014-11-22 修回日期:2014-12-19 发布日期:2015-01-07
  • 通讯作者: 许斌
  • 基金资助:

    国家自然科学基金(No. 21272149)和上海市教委科研创新重点(No. 14ZZ094)资助项目.

Recent Advances in Inert Bonds Activation with Isocyanides

Wang Haoa, Xu Bina,b,c   

  1. a Department of Chemistry, Shanghai University, Shanghai 200444;
    b State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032;
    c Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University, Shanghai 200062
  • Received:2014-11-22 Revised:2014-12-19 Published:2015-01-07
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 21272149), and the Innovation Program of Shanghai Municipal Education Commission (No. 14ZZ094).

Transition-metal-catalyzed C—H functionalization has attracted tremendous interest as a valuable tool for the construction of heterocycles. As a unique building block, isocyanides have been widely used in the synthesis of various nitrogen-containing heterocycles through multi-component Passerini and Ugi reactions. This review highlights the recent progress in inert bonds activation with isocyanides, including C—H bond or N—H bond insertion of isocyanides and radical oxidative annulation of isocyanides.

Key words: C—H bond activation, isocyanide, free radical reaction, insertion reaction, nitrogen heterocycles