Iodine-catalyzed 1-Aryltriazene/CS2 duo for sonochemical synthesis of 3-Sulphenylindoles employing [BMIM(SO3H)][OTf] as recyclable promoting system.

Iodine-catalyzed regioselective sulphenylation of various 3-substituted indoles using CS 2 as potential tool is demonstrated. An efficient and eco-friendly protocol has been developed to synthesize libraries of 3-sulphenyl indoles by employing CS 2 as sulphur coupling-linkage for various 1-aryltriaznes and indoles. Short reaction time, mild reaction conditions, recycle and reuse of ionic liquids (ILs) are the advantages of this methodology. A plausible reaction mechanism to narrate the exploitation of the catalytic and promoting systems is also highlights of this work.

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Publication Details

Journal
Journal of Ionic Liquids
Published
2024-12-04
DOI
https://doi.org/10.1016/j.jil.2024.100128
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.25

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article

Iodine-catalyzed 1-Aryltriazene/CS2 duo for sonochemical synthesis of 3-Sulphenylindoles employing [BMIM(SO3H)][OTf] as recyclable promoting system.

Shruti S. Malunavar, Suraj M. Sutar, Rajesh G. Kalkhambkar, Vinod S. Jadhav et al.
1 citations
Journal of Ionic Liquids
Sulfur-Based Synthesis Techniques
0.25
article

Iodine-catalyzed 1-Aryltriazene/CS2 duo for sonochemical synthesis of 3-Sulphenylindoles employing [BMIM(SO3H)][OTf] as recyclable promoting system.

Shruti S. Malunavar, Suraj M. Sutar, Rajesh G. Kalkhambkar, Vinod S. Jadhav, Athmanand Anchi, Imamhusen Jamadar
article en
1 citations

Abstract

Iodine-catalyzed regioselective sulphenylation of various 3-substituted indoles using CS 2 as potential tool is demonstrated. An efficient and eco-friendly protocol has been developed to synthesize libraries of 3-sulphenyl indoles by employing CS 2 as sulphur coupling-linkage for various 1-aryltriaznes and indoles. Short reaction time, mild reaction conditions, recycle and reuse of ionic liquids (ILs) are the advantages of this methodology. A plausible reaction mechanism to narrate the exploitation of the catalytic and promoting systems is also highlights of this work.

Journal of Ionic LiquidsVol. 5(1)
Karnatak University (IN), Sanskriti Samvardhan Mandal (IN)
Vision Group on Science and Technology
Openalex Percentile: Top 46%
Sulfur-Based Synthesis Techniques
0.25
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Iodine-catalyzed 1-Aryltriazene/CS2 duo for sonochemical synthesis of 3-Sulphenylindoles employing [BMIM(SO3H)][OTf] as recyclable promoting system. — Shruti S. Malunavar, Suraj M. Sutar, et al. · Journal of Ionic Liquids (2024) | TGRS Research Map | TGRS