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Immobilization hydroxynitrile lyase

F.L. Cabirol, U. Hanefeld, Immobilized Hydroxynitrile Lyases for Enantioselective Synthesis of Cyanohydrins Sol-Gels and Cross-Linked Enzyme Aggregates, Adv. Synth. Catal. (2006)... [Pg.126]

Nippon Shokubai Kagaku Kogyo disclosed a complementary process for the synthesis of optically active cyanohydrins. (S)-hydroxynitrile lyase derived from plants like Euphorbiaceae, Gramineae, and Olacaceae could successfully be applied to synthesize 99.9% optically active (S)-mandelonitrile (S)-175 [147]. The enzymes showed high absorption ratios when immobilized on porous inorganic material such as ceramics, silica, alumina, or silica/alumina zeolithes and were also used for the synthesis of other cyanohydrins. [Pg.310]


See other pages where Immobilization hydroxynitrile lyase is mentioned: [Pg.216]    [Pg.26]    [Pg.264]    [Pg.977]   


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