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钒催化的氧化 C(CO)-C(CO)键断裂用于 C-N 键形成:1,2-二酮和脒一锅多步转化为酰亚胺和酰胺。

Vanadium-Catalyzed Oxidative C(CO)-C(CO) Bond Cleavage for C-N Bond Formation: One-Pot Domino Transformation of 1,2-Diketones and Amidines into Imides and Amides.

机构信息

Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER) , Balanagar, Hyderabad 500037, India.

出版信息

J Org Chem. 2017 Jul 21;82(14):7332-7345. doi: 10.1021/acs.joc.7b00950. Epub 2017 Jul 5.

Abstract

A novel vanadium-catalyzed one-pot domino reaction of 1,2-diketones with amidines has been identified that enables their transformation into imides and amides. The reaction proceeds by dual acylation of amidines via oxidative C(CO)-C(CO) bond cleavage of 1,2-diketones to afford N,N'-diaroyl-N-arylbenzamidine intermediates. In the reaction, these intermediates are easily hydrolyzed into imides and amides through vanadium catalysis. This method provides a practical, simple, and mild synthetic approach to access a variety of imides as well as amides in high yields. Moreover, one-step construction of imide and amide bonds with a long-chain alkyl group is an attractive feature of this protocol.

摘要

一种新型的钒催化 1,2-二酮与脒的一锅多组分反应被发现,该反应可以将 1,2-二酮转化为酰亚胺和酰胺。该反应通过 1,2-二酮的氧化 C(CO)-C(CO)键断裂对脒进行双重酰化,从而得到 N,N'-二芳酰基-N-芳基苯甲脒中间体。在反应中,这些中间体在钒催化下很容易水解成酰亚胺和酰胺。该方法为获得各种酰亚胺和酰胺提供了一种实用、简单和温和的合成方法,产率高。此外,用长链烷基一步构建酰亚胺和酰胺键是该方案的一个吸引人的特点。

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