Visible‐Light‐Induced Three‐Component Assembly of β‐Hydroxysulfides with Alkenes and Thiosulfonates

Abstract A strategy for the synthesis of β‐hydroxysulfide derivatives via a visible‐light‐induced radical reaction of alkenes with thiosulfonates has been developed. The approach offers a convenient and environmentally friendly route for the simultaneous incorporation of Csp 3 ─O and Csp 3 ─S bonds, affording valuable polyfunctionalized alkane derivatives containing sulfur in satisfactory yields. In addition, the utility of this protocol was manifested by the late‐stage modification of several pharmaceutically relevant molecules, such as flurbiprofen, oxaprozin, febuxostat, and ibuprofen.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-07-14
DOI
https://doi.org/10.1002/ajoc.202500532
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Visible‐Light‐Induced Three‐Component Assembly of β‐Hydroxysulfides with Alkenes and Thiosulfonates

Peng Zhou, Weibing Liu, Jiang Yan-fu, Hailing Liu et al.
Asian Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Visible‐Light‐Induced Three‐Component Assembly of β‐Hydroxysulfides with Alkenes and Thiosulfonates

Peng Zhou, Weibing Liu, Jiang Yan-fu, Hailing Liu, Jiantao Zhang, Xian Jiang, Renhua Su
article en

Abstract

Abstract A strategy for the synthesis of β‐hydroxysulfide derivatives via a visible‐light‐induced radical reaction of alkenes with thiosulfonates has been developed. The approach offers a convenient and environmentally friendly route for the simultaneous incorporation of Csp 3 ─O and Csp 3 ─S bonds, affording valuable polyfunctionalized alkane derivatives containing sulfur in satisfactory yields. In addition, the utility of this protocol was manifested by the late‐stage modification of several pharmaceutically relevant molecules, such as flurbiprofen, oxaprozin, febuxostat, and ibuprofen.

Asian Journal of Organic ChemistryVol. 14(9)
Beijing Normal University (CN), Guangdong University of Petrochemical Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 87%
Sulfur-Based Synthesis Techniques
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