AgSbF<sub>6</sub> CatalyzedReduction of Nitroarenesby Phenylsilane to Anilines

AgSbF<sub>6</sub>-catalyzed activation of phenylsilane (PhSiH<sub>3</sub>) 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.

Publication Details

Journal
Figshare
Published
2025-02-21
DOI
https://doi.org/10.1021/acs.joc.4c02639.s001
Primary Topic
Nanomaterials for catalytic reactions
Type
article
Field-Weighted Citation Impact
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article

AgSbF6 CatalyzedReduction of Nitroarenesby Phenylsilane to Anilines

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Nanomaterials for catalytic reactions
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AgSbF6 CatalyzedReduction of Nitroarenesby Phenylsilane to Anilines

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Abstract

AgSbF<sub>6</sub>-catalyzed activation of phenylsilane (PhSiH<sub>3</sub>) 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.

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Openalex Percentile: Top 69%
Nanomaterials for catalytic reactions
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AgSbF<sub>6</sub> CatalyzedReduction of Nitroarenesby Phenylsilane to Anilines · Figshare (2025) | TGRS Research Map | TGRS