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Nickel-catalyzed cross-coupling of epoxides with aryltriflates: rapid and regioselective construction of aryl ketones
Chemical Communications ( IF 4.9 ) Pub Date : 2022-07-22 , DOI: 10.1039/d2cc02891c
Jinglin Qu 1 , Zijuan Yan 1 , Xuchao Wang 1 , Jun Deng 2 , Feipeng Liu 1 , Zi-Qiang Rong 1
Affiliation  

Aryl ketones are one of the most important classes of organic compounds, and widely present in various pharmacological compounds, biologically active molecules and functional materials. Presented herein is a facile synthetic method for the construction of ketones via Ni-catalyzed cross coupling of epoxides with aryltriflates. A range of easily accessible epoxides can be highly regioselectively converted to the corresponding aryl ketones with good yields in a redox neutral fashion.

中文翻译:

镍催化环氧化物与芳基三氟甲磺酸酯的交叉偶联:芳基酮的快速区域选择性构建

芳基酮是一类最重要的有机化合物,广泛存在于各种药理化合物、生物活性分子和功能材料中。本文介绍了一种通过Ni 催化的环氧化物与芳基三氟甲磺酸酯的交叉偶联来构建酮的简便合成方法。一系列易于获得的环氧化物可以高度区域选择性地转化为相应的芳基酮,并以氧化还原中性方式以良好的收率。
更新日期:2022-07-27
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