Publication | Closed Access
Iridium-Catalyzed Asymmetric Hydrogenation of Ketones with Accessible and Modular Ferrocene-Based Amino-phosphine Acid (f-Ampha) Ligands
101
Citations
41
References
2017
Year
Inorganic ChemistryIridium-catalyzed Asymmetric HydrogenationCross-coupling ReactionEngineeringBiochemistryNatural SciencesF-ampha Ligands-Cooh GroupOrganic ChemistryOrganometallic CatalysisCatalysisDft CalculationsChemistryHomogeneous CatalysisAsymmetric Catalysis
A series of tridentate ferrocene-based amino-phosphine acid (f-Ampha) ligands have been successfully developed. The f-Ampha ligands are extremely air stable and exhibited excellent performance in the Ir-catalyzed asymmetric hydrogenation of ketones (full conversions, up to >99% ee, and 500 000 TON). DFT calculations were performed to elucidate the reaction mechanism and the importance of the -COOH group. Control experiments also revealed that the -COOH group played a key role in this reaction.
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