Highly Chemoselective Thiocarbonyl Oxidation upon Reaction of 4-Methyl-3-phenyl-2-thiazolidinethione with Singlet Oxygen
4-Methyl-3-phenyl-2-thiazolidinethione was reacted with both photochemically and chemically generated singlet oxygen. Despite reaction conditions which were selected to favor oxidation of the sulfide group, both reactions afforded a single product arising solely from thiocarbonyl oxidation.
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Veröffentlicht in: | Spectroscopy letters 1996-09, Vol.29 (6), p.1013-1019 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | 4-Methyl-3-phenyl-2-thiazolidinethione was reacted with both photochemically and chemically generated singlet oxygen. Despite reaction conditions which were selected to favor oxidation of the sulfide group, both reactions afforded a single product arising solely from thiocarbonyl oxidation. |
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ISSN: | 0038-7010 1532-2289 |
DOI: | 10.1080/00387019608007268 |