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


Expedient synthesis of novel β-ketoesters from the Mizoroki–Heck coupling of ethyl 3-ethoxyacrylate with aryl and pyridyl halides
Authors:Jeffrey T Kohrt  Ed Conn  Robert Maguire  Stephen W Wright  Robert Singer
Institution:1. CVMED Reaction Optimization Center, Pfizer Worldwide Research and Development, Groton Laboratories, Eastern Point Road, Groton, CT 06340, United States;2. CVMED World Wide Medicinal Chemistry, Pfizer Worldwide Research and Development, Groton Laboratories, Eastern Point Road, Groton, CT 06340, United States;3. Chemical Research and Development, Pfizer Worldwide Research and Development, Groton Laboratories, Eastern Point Road, Groton, CT 06340, United States
Abstract:It is well known that β-ketoesters are useful intermediates for the synthesis of a range of heterocyclic templates. While there are many useful synthetic methods available to access these intermediates, there are still opportunities for the discovery of useful methodologies for their construction from novel starting materials. In this regard, we report on the discovery of a facile Pd-catalyzed Mizoroki–Heck coupling of ethyl 3-ethoxyacrylate with aryl and heteroaryl halides to form substituted alkoxyacrylates which can be hydrolyzed to form novel aryl and heteroaryl β-ketoesters.
Keywords:Mizoroki&ndash  Heck  Coupling  β-Ketoesters  Palladium  Catalysis
本文献已被 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