Publication | Closed Access
Direct β-Alkylation of Ketones and Aldehydes via Pd-Catalyzed Redox Cascade
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Citations
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References
2018
Year
Pd-catalyzed Redox-cascade StrategyChemical EngineeringCross-coupling ReactionEngineeringCatalytic SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisDirect β-AlkylationChemistrySimple Alkyl BromidesBiomolecular Engineering
We report a direct β-alkylation of ketones and aldehydes with simple alkyl bromides through a Pd-catalyzed redox-cascade strategy. The use of a Cu cocatalyst is important for improved efficiency. The reaction is redox-neutral, without the need for strong acids or bases. Both cyclic and acyclic ketones, as well as α-branched aldehydes, are suitable substrates for coupling with secondary and tertiary alkyl bromides. Concise formal synthesis of Zanapezil is achieved using this β-alkylation method.
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