Synthesis of Diaryl Thiosulfonates via Electrochemical Cascade S─S‐Coupling Using Arylsulfonyl Chlorides/Arylsulfinate Salts

Abstract A facile and straightforward electrochemical method for synthesizing diaryl thiosulfonates is reported. The process involves a combination of consecutive in situ electrochemical–autocatalytic processes, followed by a C─S coupling sequence, to enable the formation of diaryl thiosulfonates using either arylsulfinate salts or arylsulfonyl chlorides alone. Thus, unlike previous methods, it avoids using stoichiometric thiol or disulfide reaction partners, over‐stoichiometric promoters, metal‐based redox reagents, or catalysts, thereby minimizing the formation of undesired products and chemical waste. A range of arylsulfinate salts/arylsulfonyl chlorides was screened under the reaction conditions, yielding the corresponding diaryl thiosulfonates in moderate‐to‐good yields.

Authors

Institutions

Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-08-30
DOI
https://doi.org/10.1002/ajoc.202500499
Citations
2
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
1.87

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synthesis of Diaryl Thiosulfonates via Electrochemical Cascade S─S‐Coupling Using Arylsulfonyl Chlorides/Arylsulfinate Salts

Ajay Kumar, MADHUBALA MADHUBALA, Sushobhan Chowdhury, Manoj Kumar Yadav
2 citations
Asian Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
1.87
article

Synthesis of Diaryl Thiosulfonates via Electrochemical Cascade S─S‐Coupling Using Arylsulfonyl Chlorides/Arylsulfinate Salts

Ajay Kumar, MADHUBALA MADHUBALA, Sushobhan Chowdhury, Manoj Kumar Yadav
article en
2 citations

Abstract

Abstract A facile and straightforward electrochemical method for synthesizing diaryl thiosulfonates is reported. The process involves a combination of consecutive in situ electrochemical–autocatalytic processes, followed by a C─S coupling sequence, to enable the formation of diaryl thiosulfonates using either arylsulfinate salts or arylsulfonyl chlorides alone. Thus, unlike previous methods, it avoids using stoichiometric thiol or disulfide reaction partners, over‐stoichiometric promoters, metal‐based redox reagents, or catalysts, thereby minimizing the formation of undesired products and chemical waste. A range of arylsulfinate salts/arylsulfonyl chlorides was screened under the reaction conditions, yielding the corresponding diaryl thiosulfonates in moderate‐to‐good yields.

Asian Journal of Organic ChemistryVol. 14(10)
Guru Gobind Singh Indraprastha University (IN), Central Drug Research Institute (IN), Indian Institute of Technology Delhi (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Department of Science and Technology, Government of Rajasthan
Openalex Percentile: Top 14%
Sulfur-Based Synthesis Techniques
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.