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Iridium-Catalyzed Asymmetric Hydrosilylation of Imines Using Chiral Oxazolinyl-Phosphine Ligands
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Citations
11
References
1999
Year
Enantioselective SynthesisEngineeringChiral OxazolinylphosphinesAsymmetric HydrosilylationOrganic ChemistryOrganometallic CatalysisChemistryAsymmetric CatalysisEffective LigandsIridium-catalyzed Asymmetric HydrosilylationBiomolecular Engineering
Chiral oxazolinylphosphines are effective ligands for the Ir(I)-catalyzed asymmetric hydrosilylation of imines to afford the corresponding sec-amines with high enantioselectivities (up to 89% ee) after hydrolysis in almost quantitative yields. The structure of an Ir(I)−oxazolinylferrocenylphosphine complex was determined by X-ray analysis.
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