Green Chemistry Letters and Reviews · 2011 · 32 citations · 61 references
Natural SciencesChemical EngineeringChemistryGreen ChemistryOrganic ChemistryReaction EngineeringDisulfide Bond FormationMicrowave-assisted SynthesisOrganic SynthesisDisulfide ChemistryMicrowave Irradiation EffectsMicrowave-assisted Materials SynthesisMicrowave-assisted Organic SynthesisOrganic Oxidation Reactions
Abstract We present here a clean and fast synthesis of organic disulfides starting from thiols using glycerol as solvent under microwave irradiation. This efficient method is general for aromatic, aliphatic, and functionalized thiols, affording the corresponding disulfides in good to excellent yields after easy work up. Glycerol can be easily recovered and utilized for further oxidation reactions.
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