Publication | Closed Access
Diastereospecific and Enantioselective Access to Dispirooxindoles from Furfurylcyclobutanols by Means of a Pd-Catalyzed Arylative Dearomatization/Ring Expansion Cascade
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Citations
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References
2016
Year
Asymmetric CatalysisNovel DispirooxindolesEngineeringNatural SciencesDiversity-oriented SynthesisEnantioselective AccessOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryQuaternary Carbon CentersSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringGood Yields
We report a Pd-catalyzed arylative dearomatization/ring expansion cascade of furfurylcyclobutanols that involves a spiro π-allyl palladium intermediate and affords structurally novel dispirooxindoles containing two quaternary carbon centers in good yields with high step economy, diastereospecificity, and enantioselectivity.
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