Issue 20, 2017
From the journal:

New Journal of Chemistry

Cu-Catalyzed first direct access towards 3-sulfenylindoles from aryl halides†

N. Golzar,a   N. Nowrouzi, ORCID logo *a   M. Abbasia  and  A. M. Mehranpoura  

* Corresponding authors

a Department of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr, Iran
E-mail: nowrouzi@pgu.ac.ir

Abstract

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.

Graphical abstract: Cu-Catalyzed first direct access towards 3-sulfenylindoles from aryl halides

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Article information

DOI
https://doi.org/10.1039/C7NJ01783A
Article type
Paper
Submitted
22 May 2017
Accepted
30 Aug 2017
First published
01 Sep 2017

New J. Chem., 2017,41, 11921-11925

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Cu-Catalyzed first direct access towards 3-sulfenylindoles from aryl halides

N. Golzar, N. Nowrouzi, M. Abbasi and A. M. Mehranpour, New J. Chem., 2017, 41, 11921 DOI: 10.1039/C7NJ01783A

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