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1998 stereochemistry stereochemistry (general, optical resolution) O 0030 44 - 041 α-Amino Acidate-Ru(II) Catalysts for Asymmetric Transfer Hy- drogenation: First Utilization of α-Amino Acids as an Efficient Ligand. Ru-complexes (I) derived from potassium salts of α-amino acids and Ru 2 Cl 4 (arene) 2 prove to be efficient catalysts for the asymmetric transfer hydrogenation of ketones from alcohols. Enantiomeric excesses of the products reach 92%. — (OHTA, T.; NAKAHARA, S.; SHIGEMURA, Y.; HATTORI, K.; FURUKAWA, I.; Chem. Lett. (1998) 6, 491-492; Dep. Mol. Sci. Technol., Fac. Eng., Doshisha Univ., Tanabe, Kyoto 610-03, Japan; EN) 1

ChemInform Abstract: α-Amino Acidate-Ru(II) Catalysts for Asymmetric Transfer Hydrogenation: First Utilization of α-Amino Acids as an Efficient Ligand

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1998 stereochemistry

stereochemistry (general, optical resolution)O 0030

44 - 041α-Amino Acidate-Ru(II) Catalysts for Asymmetric Transfer Hy-drogenation: First Utilization of α-Amino Acids as an EfficientLigand. — Ru-complexes (I) derived from potassium salts of α-amino acidsand Ru2Cl4(arene)2 prove to be efficient catalysts for the asymmetric transferhydrogenation of ketones from alcohols. Enantiomeric excesses of the productsreach 92%. — (OHTA, T.; NAKAHARA, S.; SHIGEMURA, Y.; HATTORI,K.; FURUKAWA, I.; Chem. Lett. (1998) 6, 491-492; Dep. Mol. Sci. Technol.,Fac. Eng., Doshisha Univ., Tanabe, Kyoto 610-03, Japan; EN)

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