POCl 3 /Sulfoxide‐ and Acetyl Bromide/Sulfoxide‐Promoted Oxidative Sulfenylation of Indoles

A mild and rapid chemoselective sulfenylation of indoles with thiophenols has been established by the employment of sulfoxide as the oxidant and POCl 3 (phosphorus oxychloride) or AcBr (acetyl bromide) as the activator at ambient temperature. Sulfenylation of indoles at the C3 position can be achieved in the presence of POCl 3 and tetramethylene sulfoxide, while a sulfenylation/bromination cascade was reached by combining AcBr and dimethyl sulfoxide in the reaction system.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-10-13
DOI
https://doi.org/10.1002/ejoc.70901
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

POCl 3 /Sulfoxide‐ and Acetyl Bromide/Sulfoxide‐Promoted Oxidative Sulfenylation of Indoles

Hai‐Lei Cui, Ze Wang, Man Jiang, Ying Li et al.
European Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

POCl 3 /Sulfoxide‐ and Acetyl Bromide/Sulfoxide‐Promoted Oxidative Sulfenylation of Indoles

Hai‐Lei Cui, Ze Wang, Man Jiang, Ying Li, Yu Luo, Yu‐Mei Ma, Xing‐Feng Liao, Yu‐Jia Chen, Xin Yu, Jia‐Wei Ruan
article en

Abstract

A mild and rapid chemoselective sulfenylation of indoles with thiophenols has been established by the employment of sulfoxide as the oxidant and POCl 3 (phosphorus oxychloride) or AcBr (acetyl bromide) as the activator at ambient temperature. Sulfenylation of indoles at the C3 position can be achieved in the presence of POCl 3 and tetramethylene sulfoxide, while a sulfenylation/bromination cascade was reached by combining AcBr and dimethyl sulfoxide in the reaction system.

European Journal of Organic Chemistry
Chongqing University of Arts and Sciences (CN)
Openalex Percentile: Top 25%
Sulfur-Based Synthesis Techniques
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