Organic Letters · 2008 · 156 citations · 32 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsHeterogeneous CatalysisMetal CatalysisEnantioselective CatalysisEnantioselective Catalyst DesignEnantioselective SynthesisHydrogenationHydrogenation CatalysisHydrogenation ReactionsOrganoiridium ChemistryQuinoline Chemistry
Enantioselective hydrogenation of quinoline derivatives catalyzed by phosphine-free chiral cationic Cp*Ir(OTf)(CF 3TsDPEN) complex (CF 3TsDPEN = N-(p-trifluoromethylbenzenesulfonyl)-1,2-diphenylethylene-diamine) afforded the 1,2,3,4-tetrahydroquinoline derivatives in up to 99% ee. The reaction could be carried out with a substrate-to-catalyst molar ratio as high as 1000 in undegassed methanol and with no need for inert gas protection.
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