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Rhodium(Ⅲ)-catalyzed selective access to isoindolinones via formal [4+1] annulation of arylamides and propargyl alcohols

三价铑催化N-甲氧基苯甲酰胺与炔丙醇[4+1]环化合成异吲哚啉酮(英文)

作     者:Youwei Xu Fen Wang Songjie Yu Xingwei Li 许有伟;王芬;于松杰;李兴伟

作者机构:Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 Liaoning China University of Chinese Academy of Sciences Beijing 100049 China 

出 版 物:《Chinese Journal of Catalysis》 (催化学报(英文))

年 卷 期:2017年第38卷第8期

页      面:1390-1398页

核心收录:

学科分类:081704[工学-应用化学] 07[理学] 0817[工学-化学工程与技术] 08[工学] 070303[理学-有机化学] 0703[理学-化学] 

基  金:supported by the Dalian Institute of Chemical Physics,Chinese Academy of Sciences the National Natural Science Foundation of China (21525208,21472186)~~ 

主  题:Rhodium C-H activation [4+1] annulation Propargyl alcohol Isoindolinones 

摘      要:A mild and efficient oxidative synthesis of isoindolinones has been realized by Rh(III)‐catalyzed C?H activation of benzamides and[4+1]coupling with propargyl *** coupling system proceeds with broad substrate scope and mild conditions and provides a new approach to access the useful skeleton ofγ‐lactams with a stereogenic center.

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