Copper-catalyzed alkynyldisulfuration of arynes: efficient access to unsymmetrical disulfides

This article investigates a copper-catalyzed alkynyl disulfuration reaction of arynes formed in situ that generates o -alkynyl aryl disulfides via the formation of one C–C bond and one C–SS bond in one pot.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-11-05
DOI
https://doi.org/10.1039/d4qo01844c
Citations
5
Primary Topic
Child Development and Digital Technology
Type
article
Field-Weighted Citation Impact
10.48
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article

Copper-catalyzed alkynyldisulfuration of arynes: efficient access to unsymmetrical disulfides

Chen‐Ho Tung, Shuai Huang, Yuekai Li, Zhenghu Xu et al.
5 citations
Organic Chemistry Frontiers
Child Development and Digital Technology
10.48
article

Copper-catalyzed alkynyldisulfuration of arynes: efficient access to unsymmetrical disulfides

Chen‐Ho Tung, Shuai Huang, Yuekai Li, Zhenghu Xu, Xin Li, Yumin Zhang
article en
5 citations

Abstract

This article investigates a copper-catalyzed alkynyl disulfuration reaction of arynes formed in situ that generates o -alkynyl aryl disulfides via the formation of one C–C bond and one C–SS bond in one pot.

Organic Chemistry FrontiersVol. 12(2)
Shandong University (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN), Qilu Hospital of Shandong University (CN)
Openalex Percentile: Top 2%
Child Development and Digital Technology
10.48
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