不同氟源苯乙烯的电化学直接氟化功能化:获得氟烷基衍生物。

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC The Journal of Organic Chemistry Pub Date : 2024-06-14 DOI:10.1021/acs.joc.4c00722
Boao Li, Xiaojian Liao, Linzi Wen, Mengyao Mi, Xiwen Xing, Pengju Feng* and Shihai Xu*, 
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引用次数: 0

摘要

一种温和的苯乙烯电化学氧化氟官能化方案已经得到证实。该反应在无金属、无外部氧化剂和无催化剂的条件下进行,从而可以获得多种有用的合成氟烷基衍生物,如β-氟砜/氟甲基、氟硫氰化和乙烯基磺酰基衍生物。此外,CsF 被证明是这种电化学氟官能化转化的适当氟源。
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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Electrochemically Direct Fluorination Functionalization of Styrenes with Different Fluorine Source: Access to Fluoroalkyl Derivatives

A mild protocol for electrochemically oxidative fluorodifunctionalization of styrenes has been demonstrated. The reaction proceeds under metal, external oxidant, and catalyst free conditions, allowing tunable access to a wide variety of synthetically useful fluoroalkyl derivatives, such as β-fluorosulfone/fluoromethyl, fluorothiocyanation, and vinylsulfonyl derivatives. Moreover, CsF was shown to be the proper fluorine source for this electrochemical fluorodifunctionalization transformation.

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来源期刊
The Journal of Organic Chemistry
The Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: The Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
期刊最新文献
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