首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Palladium-catalyzed cascade synthesis of spirocyclic oxindoles via regioselective C2-H arylation and C8-H alkylation of naphthalene ring
Authors:Xiai Luo  Wenguang Li  Haiyan Lu  Guobo Deng  Yuan Yang  Chunming Yang  Yun Liang
Institution:1. National & Local Joint Engineering Laboratory for New Petro-chemical Materials and Fine Utilization of Resources, Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research, Ministry of Education, Key Laboratory of the Assembly and Application of Organic Functional Molecules of Hunan Province, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China;2. Hunan University of Medicine, Huaihua 418000, China
Abstract:A simultaneous C2-H arylation and C8-H alkylation of naphthalene ring has been achieved by palladiumcatalyzed cascade reaction of N-(2-halophenyl)-2-(naphthalen-1-yl)acrylamides with aryl iodides,which provides an efficient method for synthesizing various aryl-substituted spirocyclic oxindoles.The protocol enables three C-C bonds formation via an intramolecular Heck reaction and sequentially regioselective C-H bond activation.
Keywords:Palladium-catalyzed  Cascade reaction  Regioselective C-H activation  Naphthalene ring  Spirocyclic oxindoles
本文献已被 CNKI ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号