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Dual Amine and Palladium Catalysis in Diastereo- and Enantioselective Allene Carbocyclization Reactions
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Citations
32
References
2012
Year
Diarylprolinol-based OrganocatalystsAsymmetric CatalysisChemical EngineeringNovel OrganocatalystsEngineeringDual AmineOrganic ChemistryEnamine IntermediateCatalytic Asymmetric VariantCatalysisStereoselective SynthesisChemistryOrganometallic CatalysisPalladium CatalysisEnantioselective Synthesis
A pyrrolidine and Pd catalyzed diastereoselective carbocyclization of aldehyde and ketone-linked allenes has been developed. The cooperative organo/metal-catalyzed cyclization reaction, which presumably proceeds via an enamine intermediate, is efficient and broad in scope. Also, it has been extended to a catalytic asymmetric variant using diarylprolinol-based organocatalysts to afford substituted cyclopentane and pyrrolidine reaction products in up to 82% ee.
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