1.1: RuCl2[(S)-(DM-SEGPHOS)][(S)-DAIPEN]; hydrogen; potassium tert-butylate / isopropyl alcohol / 40 h / 25 °C / 5171.62 Torr / |Glovebox 2.1: Dess-Martin periodane / dichloromethane / 0.75 h / 20 °C 3.1: dimethylsulfoxide-d6 / 0.5 h 4.1: aq. buffer / 0.25 h / |Inert atmosphere; |Irradiation 5.1: potassium tert-butylate / tetrahydrofuran / 0.75 h / 0 °C 5.2: 2 h / 3 - 20 °C 6.1: RuCl2[(S)-(DM-SEGPHOS)][(S)-DAIPEN]; hydrogen; potassium tert-butylate / isopropyl alcohol / 40 h / 25 °C / 5171.62 Torr / |Glovebox 7.1: Dess-Martin periodane / dichloromethane / 0.75 h / 20 °C 8.1: dimethylsulfoxide-d6 / 0.5 h 9.1: aq. buffer / 0.25 h / |Inert atmosphere; |Irradiation View Scheme

copper 1. THF, 25 deg C, 40min; 2. 30min; Yield given. Multistep reaction;

copper 1. THF, 25 deg C, 40min; 2. 30min; Yield given. Multistep reaction;

aluminium trichloride Friedels-Crafts benzoylation; Heating;

sodium lauryl sulfate in water Irradiationirrad. of 2,4-diphenylpentan-3-one; var. alkyl sulphate micelles; Product distributionMechanism;

sodium lauryl sulfate in water Irradiationother labelled chiral MDB's, var. sodium alkyl sulfates; effect of the micelle size, magnetic isotope effect, efficiency of isotope separation; Mechanism;

1: thionyl chloride 2: 15 percent / AlCl3 / Heating View Scheme

1: AlCl3 2: AlCl3 View Scheme

1: dimethylsulfoxide-d6 / 0.5 h 2: aq. buffer / 0.25 h / |Inert atmosphere; |Irradiation View Scheme

boron trifluoride