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NIS‐Catalyzed Reactions: Amidation of Acetophenones and Oxidative Amination of Propiophenones
144
Citations
43
References
2012
Year
Chemical EngineeringNovel OrganocatalystsEngineeringSingle-step AminationAcetophenone DerivativesOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryOxidative AminationHeterocycle ChemistryPharmacologyAsymmetric CatalysisEnantioselective SynthesisCatalytic SynthesisPropiophenone Derivatives
Single-step amination: the N-iodosuccinimide (NIS)-catalyzed amidation of acetophenone derivatives by using tert-butylhydroperoxide (TBHP) as an oxidant is presented. A variety of acetyl derivatives of heterocyclic compounds were easily converted to their corresponding ketoamides under these conditions. A new, NIS-catalyzed amination of propiophenone and its derivatives in the presence of TBHP to furnish the corresponding 2-aminoketone derivatives is the first reported single-step amination of propiophenone derivatives.
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