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EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.38synthesis (R)-benzoin is synthesized from benzaldehyde using the most stable variant immobilized in packed-bed reactors via the SpyCatcher/SpyTag system. Over a period of seven days, (R)-benzoin is produced with a stable spacetime-yield of 9.3 mmol/l and day -, 762916
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.38synthesis application of benzaldehyde lyase as a heterogeneous catalyst in the continuous synthesis (in a packed bed in a continously operated plug flow reactor for over 140 h) of the chiral 2-hydroxy ketone (R)-2-hydroxy-1-phenyl-propanone -, 666954
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.38synthesis stereoselective synthesis of novel benzoins catalysed by benzaldehyde lyase in a gel-stabilised two-phase system. (R)-1,2-di(3-furanyl)-2-hydroxyethanone, (R)-2-hydroxy-1,2-di(3-thienyl) ethanone, (R)-1,2-di(4-ethoxyphenyl)-2-hydroxyethanone, (R)-1,2-di(3-ethoxyphenyl)-2-hydroxyethanone, (R)-2-hydroxy-1,2-di(3-tolyl)ethanone, and (R)-1,2-di(benzofuran-2-yl)-2-hydroxyethanone are prepared with yields up to 31.8% and enantiomeric excess of more than 99% 666957
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.38synthesis the enzyme is a tool in chemoenzymatic synthesis of chiral alpha-hydroxyketones 690982
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