Publication | Closed Access
Asymmetric Synthesis of 1-Aryl-1,2-ethanediols from Arylacetylenes by Palladium-Catalyzed Asymmetric Hydrosilylation as a Key Step
103
Citations
8
References
2002
Year
Key StepChiral Monophosphine-palladium ComplexChemical EngineeringCross-coupling ReactionEngineeringDouble HydrosilylationAsymmetric SynthesisPalladium-catalyzed Asymmetric HydrosilylationOrganic ChemistryOrganometallic CatalysisCatalysisSynthetic ChemistryChemistryAsymmetric CatalysisHydrogen PeroxideEnantioselective SynthesisBiomolecular Engineering
Double hydrosilylation of arylacetylenes with trichlorosilane catalyzed first by platinum and second by a chiral monophosphine-palladium complex generated the corresponding 1,2-bis(silyl)-1-arylethanes, the oxidation of which with hydrogen peroxide gave 1-aryl-1,2-diols of high enantiomeric purity (94-98% ee) in high yields.
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