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使用氨基甲酰叠氮化物通过铱催化的C-H酰胺化反应合成不对称脲

Ir-Catalyzed C-H Amidation Using Carbamoyl Azides for the Syntheses of Unsymmetrical Ureas.

作者信息

Yoo Kwangho, Lee Jooyeon, Park Myung Hwan, Kim Youngjo, Kim Hyun Jin, Kim Min

机构信息

Department of Chemistry, Chungbuk National University, Cheongju 28644, Korea.

Department of Chemistry Education, Chungbuk National University, Cheongju 28644, Korea.

出版信息

J Org Chem. 2020 May 1;85(9):6233-6241. doi: 10.1021/acs.joc.0c00659. Epub 2020 Apr 21.

Abstract

An iridium-catalyzed C-H amidation for the syntheses of unsymmetrical urea was developed using carbamoyl azides (R(R')N-C(O)-N) as the nitrogen source. A combination of iridium and silver gave an active catalyst for C-N bond formation. A variety of urea derivatives were synthesized using carbamoyl azides with only dinitrogen byproducts. Finally, the use of the transient directing group strategy with carbamoyl azides extended the substrate scope of the catalytic C-H amidation to yield aldehyde-containing unsymmetrical ureas.

摘要

开发了一种铱催化的C-H酰胺化反应,用于合成不对称脲,该反应使用氨基甲酰叠氮化物(R(R')N-C(O)-N)作为氮源。铱和银的组合产生了一种用于形成C-N键的活性催化剂。使用氨基甲酰叠氮化物仅生成二氮副产物,合成了多种脲衍生物。最后,将氨基甲酰叠氮化物的瞬态导向基团策略用于催化C-H酰胺化反应,扩展了底物范围,从而生成含醛的不对称脲。

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