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Palladium-Catalyzed Dehydrogenative β′-Functionalization of β-Keto Esters with Indoles at Room Temperature
139
Citations
37
References
2012
Year
Room Temperatureβ-Keto EstersEngineeringBiochemistryIndole PartnerIndoles ProceedsNatural SciencesCatalytic SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisMild Palladium CatalysisChemistryAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringPalladium-catalyzed Dehydrogenative β′-Functionalization
The dehydrogenative β'-functionalization of α-substituted β-keto esters with indoles proceeds with high regioselectivities (C3-selective for the indole partner and β'-selective for the β-keto ester) and good yields under mild palladium catalysis at room temperature with a variety of oxidants. Two possible mechanisms involving either late or early involvement of indole are presented.
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