Publication | Closed Access
Sequential Rhodium/Palladium Catalysis: Enantioselective Formation of Dihydroquinolinones in the Presence of Achiral and Chiral Ligands
27
Citations
53
References
2014
Year
Chiral LigandsChemical EngineeringCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisSequential Rhodium/palladium CatalysisSequential Rh/pd CatalysisRhodium/palladium CatalysisOrganic ChemistryOrganometallic CatalysisCatalysisEnantioselective FormationChemistryDomino SequenceAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
Abstract Compatible combinations of achiral and chiral ligands can be used in rhodium/palladium catalysis to achieve highly enantioselective domino reactions. The difference in rates of catalysis and minimal effects of ligand interference confer control in the domino sequence. The “all‐in‐one” 1,4‐conjugate arylation and CN cross‐coupling through sequential Rh/Pd catalysis provides access to enantioenriched dihydroquinolinone building blocks.
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