Regioselective Thiolation of Indole to Construct 3-Arylthioindoles

: A practical and novel approach for the regioselective synthesis of 3-arylthioindole derivatives has been accomplished using a combination of indole substrates with p-toluene sulfonyl hydrazide. This methodology employs NIS as the oxidant and PPh3 as the reductant to give the desired 3-arylthioindoles in good to excellent yields. This method offers several advantages, including simplicity, operational ease, and broad substrate scope.

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Publication Details

Journal
Current Organic Chemistry
Published
2024-08-20
DOI
https://doi.org/10.2174/0113852728313866240807175713
Citations
1
Primary Topic
Synthesis of heterocyclic compounds
Type
article
Field-Weighted Citation Impact
0.25

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article

Regioselective Thiolation of Indole to Construct 3-Arylthioindoles

Rohit Kumar, Anushka Raj Yadav, Vikas Yadav, Virendra Prasad et al.
1 citations
Current Organic Chemistry
Synthesis of heterocyclic compounds
0.25
article

Regioselective Thiolation of Indole to Construct 3-Arylthioindoles

Rohit Kumar, Anushka Raj Yadav, Vikas Yadav, Virendra Prasad, Mitushree Ghosh
article en
1 citations

Abstract

: A practical and novel approach for the regioselective synthesis of 3-arylthioindole derivatives has been accomplished using a combination of indole substrates with p-toluene sulfonyl hydrazide. This methodology employs NIS as the oxidant and PPh3 as the reductant to give the desired 3-arylthioindoles in good to excellent yields. This method offers several advantages, including simplicity, operational ease, and broad substrate scope.

Current Organic ChemistryVol. 29(2)
Banaras Hindu University (IN)
Science and Engineering Research Board
Openalex Percentile: Top 49%
Synthesis of heterocyclic compounds
0.25
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