. . "P(GD203/08/H032), P(KAN400720701)" . "RIV/60461373:22310/08:00020032!RIV09-AV0-22310___" . . "Immobilisation of organometallic Ru or Rh complexes on various supports significantly limits their performance in enantioselective hydrogenation reactions as chiral-active catalysts. \u03B2-Hydroxyesters are often used as precursors of biological active substances. High values of enantioselectivity are usually referred to as the most requested product?s parameter. It might be generally achieved by using homogeneous optically pure complex organometallic catalysts. However, the subsequent separation seeking their effective repeated use is not a simple task. Immobilization of such catalysts onto various solid matrixes is, however, also quite difficult. On the other hand ionic liquids (ILs) due to their attractive immobilization capability might be regarded as promising alternatives to these heterogeneous systems."@en . "4"^^ . "Bartek, Luk\u00E1\u0161" . . . "2"^^ . . . . "Bratislava" . "\u0160trbsk\u00E9 Pleso, Slovakia" . "Quarternary ammonium salts as reaction media for asymmetric hydrogenation of -ketoesters" . . "Flori\u0161, Tom\u00E1\u0161" . . "7"^^ . . "Kvartern\u00ED amoniov\u00E9 soli jako reak\u010Dn\u00ED medium pro asymetrick\u00E1 hydrogenace b-ketoester\u016F"@cs . . "RIV/60461373:22310/08:00020032" . "978-80-227-2923-9" . "391280" . "Drobek, Martin" . . "asymmetric hydrogenation; ionic liquids; immobilized catalyst"@en . "Slovensk\u00E1 technick\u00E1 univerzita v Bratislave" . "Kluso\u0148, Petr" . "9th Pannonian International Symposium on Catalysis" . "Quarternary ammonium salts as reaction media for asymmetric hydrogenation of -ketoesters"@en . "22310" . "Quarternary ammonium salts as reaction media for asymmetric hydrogenation of -ketoesters" . . "Kvartern\u00ED amoniov\u00E9 soli jako reak\u010Dn\u00ED medium pro asymetrick\u00E1 hydrogenace b-ketoester\u016F"@cs . . "[AAB7FAA47694]" . "2008-09-08+02:00"^^ . "Immobilisation of organometallic Ru or Rh complexes on various supports significantly limits their performance in enantioselective hydrogenation reactions as chiral-active catalysts. \u03B2-Hydroxyesters are often used as precursors of biological active substances. High values of enantioselectivity are usually referred to as the most requested product?s parameter. It might be generally achieved by using homogeneous optically pure complex organometallic catalysts. However, the subsequent separation seeking their effective repeated use is not a simple task. Immobilization of such catalysts onto various solid matrixes is, however, also quite difficult. On the other hand ionic liquids (ILs) due to their attractive immobilization capability might be regarded as promising alternatives to these heterogeneous systems." . "Kvartern\u00ED amoniov\u00E9 soli jako reak\u010Dn\u00ED medium pro asymetrick\u00E1 hydrogenace b-ketoester\u016F"@cs . "Quarternary ammonium salts as reaction media for asymmetric hydrogenation of -ketoesters"@en . . . .