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通过铜催化的Chan-Evans-Lam反应实现氨基苯甲酰胺的化学选择性N-芳基化反应。

Chemoselective N-arylation of aminobenzamides via copper catalysed Chan-Evans-Lam reactions.

作者信息

Liu Shuai, Zu Weisai, Zhang Jinli, Xu Liang

机构信息

School of Chemistry and Chemical Engineering/Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, Shihezi University, Shihezi, 832003, China.

出版信息

Org Biomol Chem. 2017 Nov 15;15(44):9288-9292. doi: 10.1039/c7ob02491f.

Abstract

Chemoselective N-arylation of unprotected aminobenzamides was achieved via Cu-catalysed Chan-Evans-Lam cross-coupling with aryl boronic acids for the first time. Simple copper catalysts enable the selective arylation of amino groups in ortho/meta/para-aminobenzamides under open-flask conditions. The reactions were scalable and compatible with a wide range of functional groups.

摘要

首次通过铜催化的Chan-Evans-Lam交叉偶联反应,实现了未保护氨基苯甲酰胺的化学选择性N-芳基化反应。简单的铜催化剂能够在敞口烧瓶条件下,实现邻/间/对氨基苯甲酰胺中氨基的选择性芳基化反应。该反应具有可扩展性,并且与多种官能团兼容。

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