Copper-Catalyzed Sulfonamidation of N,N-Dimethyl Formamide via C(sp3)─H Bond Functionalization

IF 2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Arti Ramani, Eeshwaraiah Begari, Togati Naveen
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引用次数: 0

Abstract

We have developed a novel strategy for the direct sulfonamidation of N,N-dimethyl formamide through a copper-catalyzed C(sp3)─H functionalization reaction. This method represents a significant advancement in the field, as it does not require any exogenous acid or base, and the reaction can be completed within 2 h. A variety of N-formamidomethylated sulfonamides were synthesized in moderate to high yields. Hitherto, no prior reports have been found in the literature for the sulfonamidation of N,N-dimethyl formamide, making this reaction an important breakthrough in synthetic organic chemistry.

Abstract Image

Abstract Image

铜催化C(sp3)─氢键功能化N,N-二甲基甲酰胺磺化反应
我们开发了一种通过铜催化的C(sp3)─H功能化反应直接磺化N,N-二甲基甲酰胺的新策略。该方法不需要任何外源酸或碱,反应可在2 h内完成,是该领域的一大进步。我们以中高收率合成了多种n -甲酰胺甲基化磺胺。迄今为止,文献中未见N,N-二甲基甲酰胺磺化反应的报道,该反应是合成有机化学的重要突破。
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来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
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