Molbank
(Feb 2024)
2-Benzoyl-4-phenyl-1,2,5-thiadiazol-3(2<i>H</i>)-one 1,1-Dioxide
Emmanouil Broumidis,
Samuel B. H. Patterson,
Georgina M. Rosair,
Panayiotis A. Koutentis,
Andreas S. Kalogirou
Affiliations
Emmanouil Broumidis
Institute of Chemical Sciences, School of Engineering & Physical Sciences, Heriot-Watt University, Edinburgh EH14 4AS, UK
Samuel B. H. Patterson
Institute of Chemical Sciences, School of Engineering & Physical Sciences, Heriot-Watt University, Edinburgh EH14 4AS, UK
Georgina M. Rosair
Institute of Chemical Sciences, School of Engineering & Physical Sciences, Heriot-Watt University, Edinburgh EH14 4AS, UK
Panayiotis A. Koutentis
Department of Chemistry, University of Cyprus, P.O. Box 20537, Nicosia 1678, Cyprus
Andreas S. Kalogirou
Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P.O. Box 22006, Nicosia 1516, Cyprus
DOI
https://doi.org/10.3390/M1774
Journal volume & issue
Vol. 2024,
no. 1
p.
M1774
Abstract
Read online
3,5-Diphenyl-4H-1,2,6-thiadiazin-4-one treated with meta-chloroperoxybenzoic acid undergoes an oxidative ring contraction to give 2-benzoyl-4-phenyl-1,2,5-thiadiazol-3(2H)-one 1,1-dioxide in a 29% yield, the structure of which is supported by single-crystal X-ray diffraction analysis and the available spectroscopic data.
Keywords
WeChat QR code
Close