4.6 Article

New aminotetrazole derivatives as hydrogen bonding catalysts. A green and selective oxidation of organosulphides with H2O2 in H2O

Journal

NEW JOURNAL OF CHEMISTRY
Volume 38, Issue 8, Pages 3622-3629

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4nj00530a

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Funding

  1. MIUR, Rome
  2. University of Cagliari (National Project 'Stereoselezione in Sintesi Organica Metodologie ed Applicazioni')
  3. FIRB
  4. PRIN CINM-PIS
  5. R.A.S.
  6. 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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