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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 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/c5gc00642b |