Issue 6, 2015

Visible-light-mediated difunctionalization of styrenes: an unprecedented approach to 5-aryl-2-imino-1,3-oxathiolanes

Abstract

The visible-light-induced straightforward synthesis of 5-aryl-2-imino-1,3-oxathiolanes from styrenes and ammonium thiocyanate is reported. The protocol utilizes air (O2) and visible light as green reagents and eosin Y as an organophotoredox catalyst. The reaction involves the formation of C–S bonds followed by intramolecular C–O heterocyclization in a one-pot procedure at room temperature.

Graphical abstract: Visible-light-mediated difunctionalization of styrenes: an unprecedented approach to 5-aryl-2-imino-1,3-oxathiolanes

Supplementary files

Article information

Article type
Paper
Submitted
25 Mar 2015
Accepted
21 Apr 2015
First published
21 Apr 2015

Green Chem., 2015,17, 3515-3520

Visible-light-mediated difunctionalization of styrenes: an unprecedented approach to 5-aryl-2-imino-1,3-oxathiolanes

A. K. Yadav and L. D. S. Yadav, Green Chem., 2015, 17, 3515 DOI: 10.1039/C5GC00642B

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