Abstract
Upon UV-irradiation in chloroform solution, some of the 2,4,4,6-tetrasubstituted-4H-thiopyran-1-oxides underwent deoxygenation to give the corresponding 4H-thiopyrans in good yields together with the corresponding 4Hthiopyran- 1,1-dioxides as minor components. Moreover, in benzene as an aromatic solvent oxenoid functionalization was observed.
Keywords: 4H-Thiopyran-1-oxides, photodeoxygenation, oxenoid functionalization
Letters in Organic Chemistry
Title: 4H-Thiopyran-1-Oxides. Photochemical Deoxygenation and Oxenoid Reactivity
Volume: 3 Issue: 2
Author(s): Farnaz Jafarpour and Hooshang Pirelahi
Affiliation:
Keywords: 4H-Thiopyran-1-oxides, photodeoxygenation, oxenoid functionalization
Abstract: Upon UV-irradiation in chloroform solution, some of the 2,4,4,6-tetrasubstituted-4H-thiopyran-1-oxides underwent deoxygenation to give the corresponding 4H-thiopyrans in good yields together with the corresponding 4Hthiopyran- 1,1-dioxides as minor components. Moreover, in benzene as an aromatic solvent oxenoid functionalization was observed.
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Cite this article as:
Jafarpour Farnaz and Pirelahi Hooshang, 4H-Thiopyran-1-Oxides. Photochemical Deoxygenation and Oxenoid Reactivity, Letters in Organic Chemistry 2006; 3 (2) . https://dx.doi.org/10.2174/157017806775224242
DOI https://dx.doi.org/10.2174/157017806775224242 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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