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Phenylselenylation of Ethers using Diphenyl Diselenide–Tributylphosphine–Molecular Oxygen System under Mild Reaction Conditions
Asian Journal of Organic Chemistry ( IF 2.7 ) Pub Date : 2018-03-05 , DOI: 10.1002/ajoc.201800026
Ryota Sano 1 , Asaki Kudo 1 , Tetsu Tsubogo 1 , Hiromi Uchiro 1
Affiliation  

An efficient method for phenylselenylation of ethers using a diphenyl diselenide–tributylphosphine–molecular oxygen system has been successfully developed. The reactions proceed under mild conditions in good to high yield. A plausible reaction mechanism for the phenylselenylation via C(sp3)−H activation was also proposed, and a tributylphosphonium peroxide radical was assumed as an important intermediate in the C(sp3)−H activation.

中文翻译:

在温和的反应条件下,使用二苯二硒化物-三丁基膦-分子氧系统进行醚的苯甲磺酰化

已经成功开发了使用二苯二硒化物-三丁基膦-分子氧系统对醚进行苯硒基化的有效方法。反应在温和的条件下以高至高收率进行。还提出了通过C(sp 3)-H活化进行苯硒基化的合理反应机理,并假定过氧化三丁基phosph自由基是C(sp 3)-H活化的重要中间体。
更新日期:2018-03-05
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