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Palladium-Catalyzed Picolinamide-Directed Alkylation of Unactivated C(sp<sup>3</sup>)–H Bonds with Alkyl Iodides
376
Citations
47
References
2013
Year
Chemical EngineeringPrimary Alkyl IodidesEngineeringCross-coupling ReactionNatural SciencesDiversity-oriented SynthesisAvailable AmineCatalytic SynthesisOrganic ChemistryPalladium CatalysisOrganometallic CatalysisCatalysisChemistryPalladium-catalyzed Picolinamide-directed AlkylationSynthetic ChemistryBiomolecular Engineering
We report an efficient method for the alkylation of γ-C(sp(3))-H bonds of picolinamide-protected aliphatic amine substrates with primary alkyl iodides via palladium catalysis. Ag(2)CO(3) and dibenzyl phosphate, (BnO)(2)PO(2)H, are critical promoters of this reaction. These reactions provide a convenient and straightforward method for the preparation of high-value N-containing products from readily available amine and alkyl iodide precursors.
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