AgSbF6 Catalyzed Reduction of Nitroarenes by Phenylsilane to Anilines

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Priyabrata Biswal, Gobbilla Sai Kumar and Vadapalli Chandrasekhar*, 
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引用次数: 0

Abstract

AgSbF6-catalyzed activation of phenylsilane (PhSiH3) enables the efficient reduction of nitroarenes to produce the corresponding anilines. This methodology operates under additive-free conditions, making it highly efficient, scalable, and compatible with a wide range of electronically diverse nitroarenes. The utility of this method is exemplified by employing a cheap, commercially available metal catalyst for the facile synthesis of various anilines. Furthermore, the methodology has been extended to the synthesis of intermediates for drug molecules, demonstrating its broad applicability.

Abstract Image

AgSbF6催化苯硅烷还原硝基芳烃生成苯胺
agsbf6催化的苯基硅烷(PhSiH3)活化使硝基芳烃有效还原生成相应的苯胺。该方法在无添加剂的条件下运行,使其高效,可扩展,并与各种电子多样的硝基芳烃兼容。该方法的实用性通过采用一种廉价的、市售的金属催化剂来方便地合成各种苯胺来举例说明。此外,该方法已扩展到药物分子中间体的合成,证明了其广泛的适用性。
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来源期刊
Journal of Organic Chemistry
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: 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.
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