化学
分子间力
肟
氨基甲酸酯
催化作用
吡啶
嘧啶
吡唑
药物化学
组合化学
酰胺
氮气
分子
立体化学
有机化学
作者
Bing Zhou,Juanjuan Du,Yaxi Yang,Huijin Feng,Yuanchao Li
出处
期刊:Organic Letters
[American Chemical Society]
日期:2013-12-26
卷期号:16 (2): 592-595
被引量:85
摘要
An unprecedented Rh(III)-catalyzed direct intermolecular C–H amidation with N-hydroxycarbamates has been developed. Different directing groups, such as pyridine, pyrimidine, pyrazole, and N-OMe oxime, can be employed in this C–H amidation process, providing valuable N-carbamate-protected arylamines (e.g., Cbz, Moz, Ac, Boc, and Fmoc). More importantly, this process may afford a new avenue for intermolecular C–H amidation where readily available N-hydroxycarbamates can be used as the nitrogen source
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