Cu-Catalyzed first direct access towards 3-sulfenylindoles from aryl halidesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nj01783a

Copper iodide has been used as a catalyst for developing a new route to 3-sulfenylindoles from the reaction of aryl halides with indole derivatives in the presence of thiourea and hexachloroethane in DMSO at 120 °C in less than an hour. The copper-catalyzed cross-coupling of indole derivatives with...

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Bibliographic Details
Main Authors: Golzar, N, Nowrouzi, N, Abbasi, M, Mehranpour, A. M
Format: Article
Language:English
Online Access:Get full text
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Summary:Copper iodide has been used as a catalyst for developing a new route to 3-sulfenylindoles from the reaction of aryl halides with indole derivatives in the presence of thiourea and hexachloroethane in DMSO at 120 °C in less than an hour. The copper-catalyzed cross-coupling of indole derivatives with aryl halides in the presence of thiourea proceeds to give 3-sulfenylindoles in DMSO at 120 °C.
ISSN:1144-0546
1369-9261
DOI:10.1039/c7nj01783a