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Triarylphosphines as Aryl Donors for Pd(II)-Catalyzed Aromatic Coupling of Oxabenzonorbornadienes
49
Citations
32
References
2015
Year
Chemical EngineeringCross-coupling ReactionEngineeringAromatic CouplingMigration AbilityOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryAryl DonorsAsymmetric CatalysisBiomolecular Engineering
A new approach was developed for Pd(II)-catalyzed aromatic coupling of oxabenzonorbornadienes with triarylphosphines as both ligands and aryl donors. Diverse functional groups including halo- (F-, Cl-, and Br-), CF3(-), and furyl groups are well tolerated. For unsymmetrical triarylphosphines, the migration ability of aryls is consistent with the electronic property of substituents and maintains the order EDG-Ar > H-Ar > EWD-Ar (EDG means electron-donating group, EWG means electron-withdrawing group). A preliminary mechanistic study was also disclosed.
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