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Asymmetric Palladium‐Catalyzed Allylic Alkylation Using Dialkylzinc Reagents: A Remarkable Ligand Effect
67
Citations
54
References
2014
Year
Diorganozinc ReagentsCross-coupling ReactionEngineeringAlkene MetathesisNatural SciencesDiversity-oriented SynthesisAllyl-palladium IntermediatesOrganic ChemistryOrganometallic CatalysisCatalysisSensitive Functional GroupsChemistryAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringRemarkable Ligand Effect
A serendipitously discovered palladium-catalyzed asymmetric allylic alkylation reaction with diorganozinc reagents, which displays broad functional group compatibility, is reported. This novel transformation hinges on a remarkable ligand effect which overrides the standard "umpolung" reactivity of allyl-palladium intermediates in the presence of dialkylzincs. Owing to its mild conditions, enantioselective allylic alkylations of racemic allylic electrophiles are possible in the presence of sensitive functional groups.
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