Publication | Closed Access
A General Method for the Suzuki−Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-ortho-substituted Biaryls in 2-Propanol at Room Temperature
529
Citations
16
References
2003
Year
Room TemperatureChemical EngineeringCross-coupling ReactionEngineeringOrtho Biaryl JunctionsAlkene MetathesisPalladacylce Pre-catalystCatalytic FormationCatalytic SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryGeneral MethodAsymmetric CatalysisSynthetic ChemistrySuzuki−miyaura Cross-coupling
The catalytic formation of di- and trisubstituted ortho biaryl junctions has been achieved using a palladacylce pre-catalyst bearing a N-heterocyclic carbene ligand. This transformation is performed at room temperature in technical grade 2-propanol.
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