Journal
NEW JOURNAL OF CHEMISTRY
Volume 38, Issue 8, Pages 3622-3629Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4nj00530a
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Funding
- MIUR, Rome
- University of Cagliari (National Project 'Stereoselezione in Sintesi Organica Metodologie ed Applicazioni')
- FIRB
- PRIN CINM-PIS
- R.A.S.
- Sardinia Regional Government
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The oxidation of organosulphides catalysed by hydrogen bonding donors derived from aminotetrazole has been studied. The oxidation reaction was performed in a H2O solution using H2O2 as a versatile, green and chemoselective new approach to sulphoxides. Sulphoxide compounds are obtained in high yields and excellent selectivity through a new and easy to perform oxidation protocol. Aminotetrazole derivatives can be recycled by filtration and reused several times without expensive purification procedures.
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