Publication | Closed Access
Transition‐Metal‐Free TEMPO Catalyzed Aerobic Oxidation of Alcohols to Carbonyls Using an Efficient Br<sub>2</sub> Equivalent under Mild Conditions
19
Citations
46
References
2013
Year
Chemical EngineeringVarious AlcoholsEngineeringCatalytic AmountCatalytic ApplicationMild ConditionsCatalytic SynthesisOrganic ChemistryCatalysisBromide‐bromate CouplingChemistryMolecular CatalysisCatalytic ProcessCarbonyls Using
Abstract An effective transition‐metal‐free catalytic system is developed for aerobic oxidations of alcohols. Using catalytic amount of bromide‐bromate coupling, H 2 SO 4 , and NaNO 2 , together with 2,2,6,6‐tetramethylpiperidine N ‐oxyl radical (TEMPO) in the presence of air, various alcohols could be converted into the corresponding aldehydes or ketones in good to excellent isolated yields under mild conditions.
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