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.