New greener approach for the Se-N bond formation

IF 1.4 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR Phosphorus, Sulfur, and Silicon and the Related Elements Pub Date : 2024-01-02 DOI:10.1080/10426507.2023.2249182
Agata J. Pacuła-Miszewska , Magdalena Obieziurska-Fabisiak , Anna Laskowska , Halina Kaczmarek , Jacek Ścianowski
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引用次数: 0

Abstract

A new greener protocol that includes the rapid and quantitative conversion of diaryl diselenides, bearing an amido function, to corresponding N-substituted benzisoselenazolones by 254 nm wavelength UV lamp irradiation is presented. This free radical Se-N bond formation was utilized for a series of diversified substrates under mild reaction conditions. Carrying out the process in an photochemically inactive solvent like acetonitrile enabled to obtain a quantitative conversion for both N-aliphatic and N-aromatic derivatives.

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形成 Se-N 键的新型绿色方法
本文介绍了一种新的绿色方案,包括通过 254 纳米波长的紫外灯照射,将带有氨基功能的二芳基二硒化物快速定量地转化为相应的 N-取代的苯并异硒唑酮。在温和的反应条件下,这种自由基 Se-N 键的形成被用于一系列不同的底物。在光化学不活跃的溶剂(如乙腈)中进行这一过程,可实现 N-脂肪族和 N-芳香族衍生物的定量转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
7.70%
发文量
103
审稿时长
2.1 months
期刊介绍: Phosphorus, Sulfur, and Silicon and the Related Elements is a monthly publication intended to disseminate current trends and novel methods to those working in the broad and interdisciplinary field of heteroatom chemistry.
期刊最新文献
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