Publication | Closed Access
Pd-Catalyzed Enantioselective Syntheses of Trisubstituted Allenes via Coupling of Propargylic Benzoates with Organoboronic Acids
122
Citations
97
References
2020
Year
Asymmetric CatalysisSynthetic PotentialsChemical EngineeringCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisChiral Allenes SynthesisTrisubstituted AllenesOrganic ChemistryCatalysisStereoselective SynthesisChemistryMultiple Chiral CentersOrganoboronic AcidsEnantioselective SynthesisBiomolecular EngineeringPropargylic Benzoates
Enabled by the newly developed ligand, Ming-Phos, the first example of palladium-catalyzed highly enantioselective coupling of racemic propargylic benzoates with organoboronic acids for chiral allenes synthesis has been developed. Excellent asymmetric induction has been achieved with a decent substrate scope. Synthetic potentials for the construction of polycyclic compounds with multiple chiral centers have been demonstrated.
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