Bis(sulfone) as Bifunctional Reagent for the Alkylarylation of Alkenes and Alkynes under Photoredox Conditions

Herein, we report a strategy for the alkylarylation of unsaturated carbon-carbon bonds, wherein bis(sulfones) serve as dual-source donors to deliver alkyl and aryl groups in a single step, redefining their reactivity paradigm. Both alkenes and alkynes undergo efficient difunctionalization with broad functional group tolerance. Mechanistic studies reveal a cascade involving deprotonation, single-electron oxidation, radical addition and Smiles rearrangement.

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Publication Details

Journal
Organic Letters
Published
2025-09-29
DOI
https://doi.org/10.1021/acs.orglett.5c03661
Citations
4
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
3.74
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article

Bis(sulfone) as Bifunctional Reagent for the Alkylarylation of Alkenes and Alkynes under Photoredox Conditions

Xin‐Hua Duan, Le Liu, Chonglong He, Min Wang et al.
4 citations
Organic Letters
Sulfur-Based Synthesis Techniques
3.74
article

Bis(sulfone) as Bifunctional Reagent for the Alkylarylation of Alkenes and Alkynes under Photoredox Conditions

Xin‐Hua Duan, Le Liu, Chonglong He, Min Wang, Qi Jiang
article en
4 citations

Abstract

Herein, we report a strategy for the alkylarylation of unsaturated carbon-carbon bonds, wherein bis(sulfones) serve as dual-source donors to deliver alkyl and aryl groups in a single step, redefining their reactivity paradigm. Both alkenes and alkynes undergo efficient difunctionalization with broad functional group tolerance. Mechanistic studies reveal a cascade involving deprotonation, single-electron oxidation, radical addition and Smiles rearrangement.

Organic LettersVol. 27(40)
Xi'an Jiaotong University (CN)
Openalex Percentile: Top 7%
Sulfur-Based Synthesis Techniques
3.74
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