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Nickel‐Catalyzed Stereospecific C−H Coupling of Benzamides with Epoxides
Authors:Shibo Xu  Kazutaka Takamatsu  Prof. Dr. Koji Hirano  Prof. Dr. Masahiro Miura
Affiliation:Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Osaka, Japan
Abstract:A Ni(OAc)2‐catalyzed C?H coupling of 8‐aminoquinoline‐derived benzamides with epoxides has been developed. The reaction proceeds with concomitant removal of the 8‐aminoquinoline auxiliary to form the corresponding 3,4‐dihydroisocoumarins directly. Additionally, the nickel catalysis is stereospecific, and the cis‐ and trans‐epoxides are converted into the corresponding cis‐ and trans‐dihydroisocoumarins with retention of configuration, which is complementary to previously reported palladium catalysis. Moreover, while still preliminary, the Curn:x-wiley:14337851:media:anie201807664:anie201807664-math-0001 ?H functionalization is also achieved in the presence of modified NiCl2 catalysts.
Keywords:C−  H coupling  epoxides  lactones  nickel  stereospecificity
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