Iodine-Catalyzed Synthesis of 3‑Arylthioindoles Employing a 1‑Aryltriazene/CS2 Combination as a New Sulfenylation Source

A practical approach for the regioselective synthesis of 3-arylthioindoles has been accomplished using a combination of 1-aryltriazene/CS2 as a new sulfenylation source. The methodology employs molecular iodine as a catalyst and is compatible with a variety of structurally diverse reactants.

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Bibliographic Details
Published in:ACS omega 2020-04, Vol.5 (13), p.7627-7635
Main Authors: Pandey, Anand Kumar, Chand, Shiv, Singh, Rahul, Kumar, Saurabh, Singh, Krishna Nand
Format: Article
Language:English
Online Access:Get full text
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Description
Summary:A practical approach for the regioselective synthesis of 3-arylthioindoles has been accomplished using a combination of 1-aryltriazene/CS2 as a new sulfenylation source. The methodology employs molecular iodine as a catalyst and is compatible with a variety of structurally diverse reactants.
ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.0c00472