Issue 29, 2015

Iodine–triphenylphosphine mediated sulfenylation of imidazoheterocycles with sodium sulfinates

Abstract

An efficient approach to sulfenyl imidazoheterocycles has been developed via iodine–triphenylphosphine mediated direct sulfenylation of imidazoheterocycles with sodium sulfinates. The reactions proceed smoothly under transition-metal-free conditions with a broad range of substrate scope, giving the desired products in moderate to excellent yields.

Graphical abstract: Iodine–triphenylphosphine mediated sulfenylation of imidazoheterocycles with sodium sulfinates

Supplementary files

Article information

Article type
Communication
Submitted
30 Dec 2014
Accepted
23 Feb 2015
First published
23 Feb 2015

RSC Adv., 2015,5, 22654-22657

Author version available

Iodine–triphenylphosphine mediated sulfenylation of imidazoheterocycles with sodium sulfinates

X. Huang, S. Wang, B. Li, X. Wang, Z. Ge and R. Li, RSC Adv., 2015, 5, 22654 DOI: 10.1039/C4RA17237J

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