<i>Ortho</i>-Hydroxy-Substituted Diaryliodonium Salts Enabled Intramolecular Aryliodonium Rearrangement in Synthesis of <i>Ortho</i>-Iodo Diaryl Ethers

A new family of <i>ortho</i>-hydroxy-substituted diaryliodonium salts was synthesized with 1-acetoxy-2-iodobenzenes, in which the acetyl group was cleaved in a one-pot synthesis. The <i>ortho</i>-hydroxyl-substituted diaryliodonium salts underwent further intramolecular aryl migration reaction, giving <i>ortho</i>-iodo diaryl ethers either with or without the presence of bases.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-15
DOI
https://doi.org/10.1021/acs.joc.4c03179
Citations
3
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
2.81

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article

Ortho-Hydroxy-Substituted Diaryliodonium Salts Enabled Intramolecular Aryliodonium Rearrangement in Synthesis of Ortho-Iodo Diaryl Ethers

Jianwei Han, Zhen‐Jiang Xu, Limin Wang, Cheng Pan et al.
3 citations
The Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
2.81
article

Ortho-Hydroxy-Substituted Diaryliodonium Salts Enabled Intramolecular Aryliodonium Rearrangement in Synthesis of Ortho-Iodo Diaryl Ethers

Jianwei Han, Zhen‐Jiang Xu, Limin Wang, Cheng Pan, Taiyou Liu
article en
3 citations

Abstract

A new family of <i>ortho</i>-hydroxy-substituted diaryliodonium salts was synthesized with 1-acetoxy-2-iodobenzenes, in which the acetyl group was cleaved in a one-pot synthesis. The <i>ortho</i>-hydroxyl-substituted diaryliodonium salts underwent further intramolecular aryl migration reaction, giving <i>ortho</i>-iodo diaryl ethers either with or without the presence of bases.

The Journal of Organic ChemistryVol. 90(16)
East China University of Science and Technology (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 11%
Oxidative Organic Chemistry Reactions
2.81
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