Publication | Closed Access
Development of Chiral Spiro P‐N‐S Ligands for Iridium‐Catalyzed Asymmetric Hydrogenation of β‐Alkyl‐β‐Ketoesters
85
Citations
38
References
2015
Year
EngineeringIridium ComplexesNatural SciencesDiversity-oriented SynthesisChiral TridentateOrganic ChemistryIridium‐catalyzed Asymmetric HydrogenationCatalysisP-n-s LigandsChemistryOrganometallic CatalysisAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
The chiral tridentate spiro P-N-S ligands (SpiroSAP) were developed, and their iridium complexes were prepared. Introduction of a 1,3-dithiane moiety into the ligand resulted in a highly efficient chiral iridium catalyst for asymmetric hydrogenation of β-alkyl-β-ketoesters, producing chiral β-alkyl-β-hydroxyesters with excellent enantioselectivities (95-99.9% ee) and turnover numbers of up to 355,000.
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