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
115
Citations
63
References
2017
Year
Cross-coupling ReactionEngineeringPalladium‐catalyzed Enantioselective SynthesisCyclohex‐2‐enone AtropisomersNatural SciencesDiversity-oriented SynthesisAryl Boronic AcidOrganic ChemistryPlatform MoleculesCatalysisBiaryl AtropisomersChemistryStereoselective SynthesisOrganometallic CatalysisPharmacologyAsymmetric CatalysisEnantioselective SynthesisEnone-based Atropisomers
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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