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Article Abstract

A practical approach for the regioselective synthesis of 3-arylthioindoles has been accomplished using a combination of 1-aryltriazene/CS 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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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144174PMC
http://dx.doi.org/10.1021/acsomega.0c00472DOI Listing

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