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通过铜催化的四组分交叉偶联反应实现马来酰亚胺的氧化氨基芳硒化反应。

Oxidative Aminoarylselenation of Maleimides via Copper-Catalyzed Four-Component Cross-Coupling.

机构信息

School of Pharmaceutical Sciences , Wenzhou Medical University , Wenzhou 325035 , People's Republic of China.

State Key Laboratory of Structural Chemistry , Fujian Institute of Research on the Structure of Matter , Chinese Academy of Sciences, Fuzhou , Fujian 350002 , China.

出版信息

Org Lett. 2019 Feb 1;21(3):745-748. doi: 10.1021/acs.orglett.8b03980. Epub 2019 Jan 14.

DOI:10.1021/acs.orglett.8b03980
PMID:30638019
Abstract

The first example of copper-catalyzed four-component coupling reaction of aryl iodides, Se powder, secondary amines, and maleimides is developed. This reaction provides an efficient and concise route to access aminoarylselenated maleimides via double C-Se bonds and C-N bond formation. The appealing features of this transformation are the use of Se powder as a selenating reagent, a green catalytic system, a wide range of substrate scope, and late-stage selenation of bioactive compounds.

摘要

发展了首例铜催化的芳基碘、硒粉、仲胺和马来酰亚胺的四组分偶联反应。该反应通过双 C-Se 键和 C-N 键形成,提供了一种高效、简洁的合成氨基芳硒代马来酰亚胺的方法。该转化具有吸引力的特点是使用硒粉作为硒化试剂、绿色催化体系、广泛的底物范围以及生物活性化合物的后期硒化。

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