<i>Ortho‐</i> Functionalized Diaryliodonium Salts: Synthesis and Reactivity

Hypervalent iodine reagents have attracted considerable attention in modern organic synthesis due to their low toxicity and versatile reactivity. Among them, ortho ‐functionalized diaryliodonium salts represent an important subclass, distinguished by their unique structural characteristics and reactivity. This review summarizes recent advances in the development of ortho ‐functionalized diaryliodonium reagents, with particular emphasis on the role of ortho ‐substituents as leaving groups or participanting moieties in reactions. Newly developed transformations are discussed alongside their mechanisms, highlighting the intramolecular interactions with the iodine(III) center.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-09-28
DOI
https://doi.org/10.1002/adsc.70135
Citations
3
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
2.81
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article

Ortho‐ Functionalized Diaryliodonium Salts: Synthesis and Reactivity

Li-Feng Chu, Jianwei Han, Limin Wang
3 citations
Advanced Synthesis & Catalysis
Oxidative Organic Chemistry Reactions
2.81
article

Ortho‐ Functionalized Diaryliodonium Salts: Synthesis and Reactivity

Li-Feng Chu, Jianwei Han, Limin Wang
article en
3 citations

Abstract

Hypervalent iodine reagents have attracted considerable attention in modern organic synthesis due to their low toxicity and versatile reactivity. Among them, ortho ‐functionalized diaryliodonium salts represent an important subclass, distinguished by their unique structural characteristics and reactivity. This review summarizes recent advances in the development of ortho ‐functionalized diaryliodonium reagents, with particular emphasis on the role of ortho ‐substituents as leaving groups or participanting moieties in reactions. Newly developed transformations are discussed alongside their mechanisms, highlighting the intramolecular interactions with the iodine(III) center.

Advanced Synthesis & CatalysisVol. 367(22)
East China University of Science and Technology (CN)
Openalex Percentile: Top 9%
Oxidative Organic Chemistry Reactions
2.81
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