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

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 (O sub(2)) and visible light as green reagents and eosin Y as an organophotoredox catalyst. The reaction involves the formation of C-S...

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Published in:Green chemistry : an international journal and green chemistry resource : GC 2015-06, Vol.17 (6), p.3515-3520
Main Authors: Yadav, Arvind K, Yadav, Lal Dhar S
Format: Article
Language:English
Subjects:
Catalysts
Formations
Reagents
Styrenes
Synthesis
Thiocyanates
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description 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 (O sub(2)) 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.
doi_str_mv 10.1039/c5gc00642b
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subjects Catalysts
Formations
Reagents
Styrenes
Synthesis
Thiocyanates
title Visible-light-mediated difunctionalization of styrenes: an unprecedented approach to 5-aryl-2-imino-1,3-oxathiolanes
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