Publication | Closed Access
Chiral Counteranions in Asymmetric Transition-Metal Catalysis: Highly Enantioselective Pd/Brønsted Acid-Catalyzed Direct α-Allylation of Aldehydes
608
Citations
9
References
2007
Year
Allyl AmineEngineeringAsymmetric Transition-metal CatalysisNatural SciencesChiral Anionic LigandDiversity-oriented Synthesisα-Branched AldehydesOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisAcid-catalyzed Direct α-AllylationEnantioselective SynthesisBiomolecular EngineeringChiral Counteranions
We have developed a highly enantioselective Pd/chiral acid-catalyzed α-allylation of α-branched aldehydes with an allyl amine as the allylating species that creates all-carbon quaternary stereogenic centers in high yields and enantioselectivities. To our knowledge, this is the first time that a chiral anionic ligand is applied for achieving asymmetric induction in a palladium-catalyzed allylic alkylation reaction.
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