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Manganese(I)‐Catalyzed Enantioselective Hydrogenation of Ketones Using a Defined Chiral PNP Pincer Ligand
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Citations
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References
2017
Year
Inorganic ChemistryChemical EngineeringEnantioselective SynthesisEngineeringBiochemistryNatural SciencesMolecular HydrogenCoordination ComplexOrganic ChemistryMolecular ComplexCatalysisDft CalculationsChemistryAsymmetric CatalysisEnantioselective HydrogenationCatalytic SynthesisAsymmetric Hydrogenation
Abstract A new chiral manganese PNP pincer complex is described. The asymmetric hydrogenation of several prochiral ketones with molecular hydrogen in the presence of this complex proceeds under mild conditions (30–40 °C, 4 h, 30 bar H 2 ). Besides high catalytic activity for aromatic substrates, aliphatic ketones are hydrogenated with remarkable selectivity (e.r. up to 92:8). DFT calculations support an outer sphere hydrogenation mechanism as well as the experimentally determined stereochemistry.
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