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Enantioselective Reduction of Ketones and Imines Catalyzed by (CN‐Box)Re<sup>V</sup>–Oxo Complexes
99
Citations
70
References
2010
Year
Chemical EngineeringEnantioselective ReductionEngineeringNovel Organocatalysts-Oxo ComplexesAllylic AlcoholsOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryMolecular CatalysisAsymmetric CatalysisProchiral KetonesEnantioselective SynthesisBiomolecular Engineering
The development and application of chiral, non-racemic Re(V)-oxo complexes to the enantioselective reduction of prochiral ketones is described. In addition to the enantioselective reduction of prochiral ketones, we report the application of these complexes to 1) a tandem Meyer-Schuster rearrangement/reduction to access enantioenriched allylic alcohols and 2) the enantioselective reduction of imines.
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