Harnessing Phenonium Ions in Synthesis

Abstract Whereas phenonium ions have been known for decades, their use in synthesis has been surprisingly scarce. This might be attributed to the difficulty in taming their formation and reactivity. However, by considering the physical‐organic properties of phenonium species, through careful design of substrates, or the use of defined reagents/promoter systems, several applications have emerged in recent years to overcome those challenges. This minireview encompasses key recent strategies to generate those highly reactive cationic intermediates in line with their physicochemical properties, with special emphasis on mechanistic aspects, regioselectivity, and functional group compatibility.

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Publication Details

Journal
Angewandte Chemie
Published
2025-09-28
DOI
https://doi.org/10.1002/ange.202516932
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
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article

Harnessing Phenonium Ions in Synthesis

David Lebœuf, Robert J. Mayer
Angewandte Chemie
Oxidative Organic Chemistry Reactions
article

Harnessing Phenonium Ions in Synthesis

David Lebœuf, Robert J. Mayer
article en

Abstract

Abstract Whereas phenonium ions have been known for decades, their use in synthesis has been surprisingly scarce. This might be attributed to the difficulty in taming their formation and reactivity. However, by considering the physical‐organic properties of phenonium species, through careful design of substrates, or the use of defined reagents/promoter systems, several applications have emerged in recent years to overcome those challenges. This minireview encompasses key recent strategies to generate those highly reactive cationic intermediates in line with their physicochemical properties, with special emphasis on mechanistic aspects, regioselectivity, and functional group compatibility.

Angewandte ChemieVol. 137(43)
Centre National de la Recherche Scientifique (FR), Technical University of Munich (DE), Université de Strasbourg (FR)
Openalex Percentile: Top 80%
Oxidative Organic Chemistry Reactions
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