Organic Process Research & Development · 2009 · 44 citations · 32 references
Natural SciencesChemical EngineeringChemistryCatalysisInorganic ChemistryOrganic ChemistryCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsCatalytic MechanismsCatalytic Reaction EngineeringCatalytic Reaction MechanismsHydrogenationHydrogenation CatalysisHydrogenation ReactionsRuthenium-catalyzed Coupling
Asymmetric hydrogenation of 3-quinuclidinone with RuBr 2 [( S, S )-xylskewphos](pica) in a base containing ethanol affords ( R )-3-quinuclidinol in 88−90% ee (XylSkewphos = 2,4-bis(di-3,5-xylylphosphino)pentane, PICA = α-picolylamine). The optical purity of the product is readily increased to >99% by recrystallization. The hydrogenation of a 4.3-kg scale with a substrate-to-catalyst molar ratio of 100 000 under 15 atm of H 2 at 30−45 °C completes in 4 h. Use of methanol or 2-propanol as a solvent decreases the catalyst efficiency. RuCl 2 (skewphos)(pica), and RuCl 2 (tolbinap)(pica) which have similar structures, are less effective for this reaction.
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Henri Doucet, Takeshi Ohkuma, Kunihiko Murata et al. · Angewandte Chemie International Edition · 1998 · 632 citations
Takeshi Ohkuma, Masatoshi Koizumi, Henri Doucet et al. · Journal of the American Chemical Society · 1998 · 404 citations
Preferential hydrogenation of aldehydes and ketones.
Takeshi Ohkuma, Hirohito Ooka, Takao Ikariya et al. · Journal of the American Chemical Society · 1995 · 381 citations