硝基苯
化学
部分
铱
催化作用
咪唑
组合化学
酰胺
有机化学
反应机理
作者
Sanjit K. Mahato,Nozomi Ohara,Shrikant M. Khake,Naoto Chatani
标识
DOI:10.1021/acscatal.1c01901
摘要
The Ir(III)-catalyzed direct α-C–H amidation of imidazole-masked aliphatic carboxylic acids with dioxazolones is reported. The presence of an imidazole moiety as a directing group is a key to the success of the reaction. The products can be easily converted to esters and amides in a simple procedure. The reaction shows a broad substrate scope for various substituted 2-acylimidazoles, as well as a variety of dioxazolone derivatives with important functional groups being tolerated. The reaction mechanism was investigated by deuterium-labeling experiments, Hammett plots, NMR, and FAB-MS, and we propose the generation of an iridium nitrene intermediate.
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