1: triethylamine / CH2Cl2 / 0.5 h / -23 °C 2: 100 percent / NaCN / dimethylsulfoxide / 5 h / 20 °C 3: KOH / ethanol / 5 h / Heating View Scheme

1: 96 percent / KOH / H2O; methanol / 4 h / Heating 2: triethylamine / CH2Cl2 / 0.5 h / -23 °C 3: 100 percent / NaCN / dimethylsulfoxide / 5 h / 20 °C 4: KOH / ethanol / 5 h / Heating View Scheme

1: 100 percent / NaCN / dimethylsulfoxide / 5 h / 20 °C 2: KOH / ethanol / 5 h / Heating View Scheme

1: 53 percent / lithium diisopropylaminde / tetrahydrofuran; hexamethylphosphoric acid triamide / 1.5 h / -108 °C 2: 70 percent Turnov. / 1M triethylaluminum, tetrakis(triphenylphosphine)palladium(0) / hexane; 1,2-dichloro-ethane / 10.5 h / 20 °C 3: 96 percent / KOH / H2O; methanol / 4 h / Heating 4: triethylamine / CH2Cl2 / 0.5 h / -23 °C 5: 100 percent / NaCN / dimethylsulfoxide / 5 h / 20 °C 6: KOH / ethanol / 5 h / Heating View Scheme

1: 70 percent Turnov. / 1M triethylaluminum, tetrakis(triphenylphosphine)palladium(0) / hexane; 1,2-dichloro-ethane / 10.5 h / 20 °C 2: 96 percent / KOH / H2O; methanol / 4 h / Heating 3: triethylamine / CH2Cl2 / 0.5 h / -23 °C 4: 100 percent / NaCN / dimethylsulfoxide / 5 h / 20 °C 5: KOH / ethanol / 5 h / Heating View Scheme

1: 1.) 2-benzenesulfonyl-3-phenyloxaziridine, pyridine / 1.) methylene dichloride, 0 grad C, 15 min, 2.) addition of hexane, 40 grad C, 30 min 2: LiOH / 1,2-dimethoxy-ethane; H2O / 3 h / 23 °C View Scheme

cell-free preparation from Convallaria majalis roots pH=7.5; 0.0833333 h; aq. buffer;

oxygen pH=7.5; 0.5 h; aq. buffer;