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镍催化的N-酰基吡咯型酰胺与有机硼试剂的交叉偶联反应。

Ni-Catalyzed cross-coupling reactions of N-acylpyrrole-type amides with organoboron reagents.

作者信息

Huang Pei-Qiang, Chen Hang

机构信息

Department of Chemistry, College of Chemistry and Chemical Engineering, and Fujian Provincial Key Laboratory of Chemical Biology, Xiamen University, Xiamen, Fujian 361005, P. R. China.

出版信息

Chem Commun (Camb). 2017 Nov 21;53(93):12584-12587. doi: 10.1039/c7cc07457c.

Abstract

The catalytic conversion of amides to ketones is highly desirable yet challenging in organic synthesis. We herein report the first Ni/bis-NHC-catalyzed cross-coupling of N-acylpyrrole-type amides with arylboronic esters to obtain diarylketones. This method is facilitated by a new chelating bis-NHC ligand. The reaction tolerates diverse functional groups on both arylamide and arylboronic ester partners including sensitive ester and ketone groups.

摘要

在有机合成中,将酰胺催化转化为酮是非常理想的,但具有挑战性。我们在此报告了首例镍/双氮杂环卡宾催化的N-酰基吡咯型酰胺与芳基硼酸酯的交叉偶联反应,以获得二芳基酮。该方法由一种新型螯合双氮杂环卡宾配体促进。该反应对芳基酰胺和芳基硼酸酯底物上的各种官能团都具有耐受性,包括敏感的酯基和酮基。

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