IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC
Babita Yadav
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引用次数: 0

摘要

通过烯醇乙酸酯与易得的磺酸钠进行氧化磺酰化反应,开发出了一种高效、一锅式、无金属催化合成 β-酮砜的方法。该方法以碘化四丁基铵(TBAI)为催化剂,以叔丁基过氧化氢(TBHP)为氧化剂,在 60°C 下进行。所开发的方案具有使用市售廉价催化剂和氧化剂、条件安全且对环境无害等优点,并提供了获得各种 β-酮砜的简便而温和的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tetrabutylammonium Iodide-Catalyzed Oxidative Coupling of Enol Acetates with Sodium Sulfinates: A Mild Access to β-Keto Sulfones

An efficient, one-pot, and metal-free catalytic synthesis of β-keto sulfones was developed through the oxidative sulfonylation of enol acetates with readily available sodium sulfinates. The protocol involves tetrabutylammonium iodide (TBAI) as a catalyst and tert-butyl hydroperoxide (TBHP) as an oxidant at 60°C. The developed protocol offers such advantages as the use of commercially available inexpensive catalysts and oxidants and safe and environmentally benign conditions, and it provides a facile and mild access to a variety of β-keto sulfones.

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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
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