Chemistry Letters · 2006 · 18 citations · 5 references
Natural SciencesChemical EngineeringChemistryCatalysisGreen ChemistryOrganic ChemistryCatalyst PreparationSolvent-free SynthesisAsymmetric ReductionsCarbonyl ReductionEnantioselective CatalysisEnantioselective ReductionEnantioselective SynthesisEnantioselectivityKetones
Abstract For the enantioselective borohydride reduction of carbonyl compounds catalyzed by the optically active ketoiminatocobalt complexes, chloroform has been employed as a unique solvent for achieving a high enantioselectivity, whereas it was found that a catalytic amount of chloroform effectively activated the present catalytic system to convert various ketones into the corresponding reduced product with a high ee in the THF solvent.
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Takushi Nagata, Kiyotaka Yorozu, Tohru Yamada et al. · Angewandte Chemie International Edition in English · 1995 · 153 citations
Catalytic Enantioselective Borohydride Reduction of <i>Ortho</i>-Fluorinated Benzophenones
Ai Kokura, Saiko Tanaka, Taketo Ikeno et al. · Organic Letters · 2006 · 47 citations
Qiuhao Chen, Luigi G. Marzilli, Nevenka Bresciani Pahor et al. · Inorganica Chimica Acta · 1988 · 18 citations