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酰胺的酰基化铃木偶联反应:通过可独立修饰的活化基团协同作用实现酰基-氮活化

Acylative Suzuki coupling of amides: acyl-nitrogen activation via synergy of independently modifiable activating groups.

作者信息

Li Xijing, Zou Gang

机构信息

Department of Fine Chemicals, East China University of Science & Technology, 130 Meilong Road, Shanghai, P. R. China.

出版信息

Chem Commun (Camb). 2015 Mar 25;51(24):5089-92. doi: 10.1039/c5cc00430f.

DOI:10.1039/c5cc00430f
PMID:25712409
Abstract

A highly efficient palladium-catalyzed acylative cross-coupling of carboxylic amides with arylboronic acids has been achieved via synergistic activation of the C(acyl)-N bond by independently modifiable activating groups. Coupling of amides features not only good functional group tolerance but also modifiable reactivities to overcome steric hindrance.

摘要

通过可独立修饰的活化基团对C(酰基)-N键的协同活化,实现了钯催化的羧酰胺与芳基硼酸的高效酰基化交叉偶联反应。酰胺的偶联不仅具有良好的官能团耐受性,而且具有可修饰的反应活性以克服空间位阻。

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