Chemoselective Phosphine-Catalyzed Reduction of Activated Carbonyls: Access to β-Hydroxy Ketones, Sulfonyls, Phosphonates, and Their Derivatives

Abstract We report a chemoselective phosphine-catalyzed reduction of activated carbonyls in ethanol. This metal-free method employs a recyclable supported catalyst, delivering high chemoselectivity (60 examples) without requiring metal complexes or borohydrides, thus providing a sustainable and practical alternative for selective carbonyl reductions.

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Publication Details

Journal
Organic Letters
Published
2026-11-02
DOI
https://doi.org/10.1021/acs.orglett.6c04339
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Chemoselective Phosphine-Catalyzed Reduction of Activated Carbonyls: Access to β-Hydroxy Ketones, Sulfonyls, Phosphonates, and Their Derivatives

Arnaud Voituriez, Solène Audor, Mathieu Zimmermann
Organic Letters
Asymmetric Hydrogenation and Catalysis
article

Chemoselective Phosphine-Catalyzed Reduction of Activated Carbonyls: Access to β-Hydroxy Ketones, Sulfonyls, Phosphonates, and Their Derivatives

Arnaud Voituriez, Solène Audor, Mathieu Zimmermann
article en

Abstract

Abstract We report a chemoselective phosphine-catalyzed reduction of activated carbonyls in ethanol. This metal-free method employs a recyclable supported catalyst, delivering high chemoselectivity (60 examples) without requiring metal complexes or borohydrides, thus providing a sustainable and practical alternative for selective carbonyl reductions.

Organic Letters
Centre National de la Recherche Scientifique (FR), Institut de Chimie des Substances Naturelles (FR), Université Paris-Saclay (FR)
Agence Nationale de la Recherche, Centre National de la Recherche Scientifique
Openalex Percentile: Top 29%
Asymmetric Hydrogenation and Catalysis
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