Palladium-Catalyzed 2,2’-Dichalcogenation of Cyclic Diaryliodonium Salts

A novel palladium-catalyzed one-step dichalcogenation of cyclic diaryliodonium salts using readily available chalcogen sources (R-SH/-SeH) is described. This method enables the efficient synthesis of a diverse range of 2,2'-dichalcogenated biaryls under mild reaction conditions and achieves modest to good yields. Notably, this strategy displays both high regioselectivity and excellent functional group tolerance. Compared with previous approaches, this system offers superior performance, providing a versatile and practical route to valuable biaryl scaffolds.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-08-26
DOI
https://doi.org/10.1021/acs.joc.5c01363
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Palladium-Catalyzed 2,2’-Dichalcogenation of Cyclic Diaryliodonium Salts

Hui Xiang, Zhaoyue Wen, Wei Chen, Pingbing Yu
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Palladium-Catalyzed 2,2’-Dichalcogenation of Cyclic Diaryliodonium Salts

Hui Xiang, Zhaoyue Wen, Wei Chen, Pingbing Yu
article en

Abstract

A novel palladium-catalyzed one-step dichalcogenation of cyclic diaryliodonium salts using readily available chalcogen sources (R-SH/-SeH) is described. This method enables the efficient synthesis of a diverse range of 2,2'-dichalcogenated biaryls under mild reaction conditions and achieves modest to good yields. Notably, this strategy displays both high regioselectivity and excellent functional group tolerance. Compared with previous approaches, this system offers superior performance, providing a versatile and practical route to valuable biaryl scaffolds.

The Journal of Organic ChemistryVol. 90(35)
Southwest Jiaotong University (CN)
Natural Science Foundation of Sichuan Province, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 83%
Sulfur-Based Synthesis Techniques
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