The Journal of Organic Chemistry · 2001 · 164 citations · 27 references
Natural SciencesChemistryCatalysisOrganic ChemistryChemical OxidationOxidation ReactionsOxidation-reduction ReactionsRedox CatalysisRedox ChemistryRedox ReactionsBaeyer-villiger OxidationCarbonyl ReductionCatalyst SelectivityCatalytic ActivityHydrogen Peroxide ChemistrySelenium Chemistry
Several diselenides were tested for catalytic activity in Baeyer-Villiger reactions with 60% aqueous hydrogen peroxide. Bis[3,5-bis(trifluoromethyl)phenyl] diselenide forms the corresponding 3,5-bis(trifluoromethyl)benzene seleninic acid in situ, which is a highly reactive and selective catalyst for the oxidation of carbonyl compounds in 1,1,1,3,3,3-hexafluoro-2-propanol, 2,2,2-trifluoroethanol, or dichloromethane.
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