Issue 8, 2014

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

Abstract

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
07 Apr 2014
Accepted
16 May 2014
First published
16 May 2014

New J. Chem., 2014,38, 3622-3629

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

F. Secci, M. Arca, A. Frongia and P. P. Piras, New J. Chem., 2014, 38, 3622 DOI: 10.1039/C4NJ00530A

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