Publication | Closed Access
Palladium‐Catalyzed Enantioselective Synthesis of 2‐Aryl Cyclohex‐2‐enone Atropisomers: Platform Molecules for the Divergent Synthesis of Axially Chiral Biaryl Compounds
28
Citations
61
References
2017
Year
EngineeringPalladium‐catalyzed Enantioselective SynthesisCyclohex‐2‐enone AtropisomersNatural SciencesDiversity-oriented SynthesisOrganic ChemistryPlatform MoleculesCatalysisBiaryl AtropisomersChemistryEnone‐based AtropisomersStereoselective SynthesisPharmacologyAsymmetric CatalysisOrganometallic CatalysisBoronic AcidEnantioselective Synthesis
Abstract The palladium‐catalyzed asymmetric synthesis of enone‐based atropisomers from 2‐iodo‐3‐methylcyclohex‐2‐enones and aryl boronic acid is reported. BoPhoz‐type phosphine–aminophosphine ligands showed superior enantioselectivity over other ligands. These cyclohexenone‐based atropisomers are useful compounds for further elaboration. The divergent synthesis of biaryl atropisomers with different ortho substituents was demonstrated.
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