化学
芳基
苯
试剂
亲核细胞
有机化学
药物化学
亲核加成
组合化学
催化作用
烷基
作者
Yuanyuan Xie,Xiaoying Jiang,Bing Gan,Ji‐Wei Liu
出处
期刊:Synlett
[Georg Thieme Verlag KG]
日期:2016-08-05
卷期号:27 (19): 2737-2741
被引量:6
标识
DOI:10.1055/s-0035-1562535
摘要
A simple and efficient method is described for the preparation of α-keto esters or amides from nitromethyl aryl ketones. In the presence of nucleophiles (alcohols or amines), the ion-supported (diacetoxyiodo)benzene-promoted sp3 C–H oxidation of nitromethyl aryl ketones proceeded efficiently under mild conditions to give the corresponding α-keto esters and amides in moderate to good yields. This is the first reported use of (diacetoxyiodo)benzene in the synthesis of α-keto esters and amides. The reaction is ecofriendly and has the advantages of mild conditions, short reaction times, and a recyclable reagent.
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