Samarium Diiodide-Mediated Radical Thioetherification of Alkyl Bromides with Disulfide Ethers

An effective samarium diiodide-mediated radical thioetherification method for alkyl bromides with disulfide ethers is reported. This method represents the first realization of radical thioetherification of alkyl bromides using a samarium diiodide-induced system. Both reaction starting materials are simple and readily available basic reagents that can be easily purchased on the market. Meanwhile, this method demonstrates excellent functional group tolerance and a broad substrate scope. Notably, this reaction system proceeds under base-free and additive-free conditions.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-04-01
DOI
https://doi.org/10.1021/acs.joc.5c03233
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Samarium Diiodide-Mediated Radical Thioetherification of Alkyl Bromides with Disulfide Ethers

Yu Liang, Chengwei Liu, Yilin Ma, Wei Zhou
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Samarium Diiodide-Mediated Radical Thioetherification of Alkyl Bromides with Disulfide Ethers

Yu Liang, Chengwei Liu, Yilin Ma, Wei Zhou
article en

Abstract

An effective samarium diiodide-mediated radical thioetherification method for alkyl bromides with disulfide ethers is reported. This method represents the first realization of radical thioetherification of alkyl bromides using a samarium diiodide-induced system. Both reaction starting materials are simple and readily available basic reagents that can be easily purchased on the market. Meanwhile, this method demonstrates excellent functional group tolerance and a broad substrate scope. Notably, this reaction system proceeds under base-free and additive-free conditions.

The Journal of Organic ChemistryVol. 91(14)
Shanghai University (CN)
Shanghai University
Openalex Percentile: Top 28%
Sulfur-Based Synthesis Techniques
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