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Palladium-Catalyzed Catellani Aminocyclopropanation Reactions with Vinyl Halides
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Citations
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References
2013
Year
Cross-coupling ReactionEnantioselective SynthesisEngineeringHeterocyclicStabilized Enolate NucleophilesOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryAsymmetric CatalysisBiomolecular EngineeringVinyl HalidesGood YieldsAliphatic Vinyl Halides
Palladium is shown to catalyze an intramolecular aminocyclopropanation of norbornenes with aliphatic vinyl halides in good yields. The reaction tolerates a variety of amine substituents and gives good results with a variety of carbocyclic and oxabicyclic [2.2.1] alkene acceptors. Notably, stabilized enolate nucleophiles were also employed in cyclopropanation reactions.
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