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基于 N-杂环卡宾的钌催化醇和仲胺的直接酰胺合成:酯的参与。

N-heterocyclic carbene based ruthenium-catalyzed direct amide synthesis from alcohols and secondary amines: involvement of esters.

机构信息

Department of Chemistry, College of Natural Sciences, Seoul National University, Seoul 151-747, Korea.

出版信息

J Org Chem. 2011 Dec 16;76(24):10005-10. doi: 10.1021/jo201756z. Epub 2011 Nov 15.

Abstract

A well-defined N-heterocyclic carbene based ruthenium complex was developed as a highly active precatalyst for the direct amide synthesis from alcohols and secondary amines. Notably, reaction of 1-hexanol and dibenzylamine afforded 60% of the corresponding amide using our catalytic system, while no amide formation was observed for this reaction with the previously reported catalytic systems. Unlike the previously reported amidation with less sterically hindered alcohols and amines, involvement of ester intermediates was observed.

摘要

开发了一种明确的基于 N-杂环卡宾的钌配合物,作为醇和仲胺直接酰胺合成的高效前催化剂。值得注意的是,使用我们的催化体系,1-己醇和二苄胺反应得到了 60%的相应酰胺,而对于之前报道的催化体系,该反应没有观察到酰胺形成。与之前报道的用位阻较小的醇和胺进行酰胺化反应不同,观察到了酯中间体的参与。

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