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Stereoselective Synthesis of Spirooxindoles by Palladium-Catalyzed Decarboxylative Cyclization of γ-Methylidene-δ-valerolactones with Isatins
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2009
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Asymmetric CatalysisNew Synthetic MethodEngineeringOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryPalladium-catalyzed Decarboxylative CyclizationSpirooxindole DerivativesPharmacologyChiral Phosphoramidite LigandSynthetic ChemistryEnantioselective Synthesis
A new synthetic method of spirooxindole derivatives has been developed by way of a palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with isatins. By employing a newly prepared phosphoramidite ligand, the reaction proceeds smoothly with excellent diastereoselectivity. Preliminary results of its application to asymmetric catalysis using a chiral phosphoramidite ligand are also described.