1: With tert.-butylhydroperoxide; FeCl3*6H2O; sodium hydroxide in water T=80°C; 10 h; 2: With hydrogenchloride in water T=20°C;

1: p-methoxy-trans-cinnamylalcohol With [Rh(acac)2(CO)2]; C17H20NOP; toluene-4-sulfonic acid in benzene T=45°C; 0.166667 h; Inert atmosphere; 2: carbon monoxide With hydrogen in benzene T=45°C; P=2585.81 Torr; 16 h; 3: With sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene in water; tert-butyl alcohol Pinnick oxidation; 6 h; Inert atmosphere; regioselective reaction;

C51H41P2Ru(1+)*C32H12BF24(1-) in toluene T=20°C; 4 h;

tellurium; Bi(NO3)3·5H2O; 5 palladium on charcoal; oxygen in methanol T=25°C; P=760.051 Torr; 8 h;

oxygen; potassium carbonate T=60°C; P=750.075 Torr; 24 h; Schlenk techniqueGreen chemistry;

C15H22Cl2N3O2PRu; glycerol; potassium hydroxide T=100°C; 6 h; Inert atmosphere;

1: 93 percent / 1 h / bath temperature 140 deg C, vapour temperature 108 deg C 2: 1.) OsO4, 2.) NaIO4 / 1.) t-BuOH, H2O, 1 h, 2.) 0 deg C, 4 h 3: 80 percent / p-TsOH / benzene / 0.25 h / Heating 4: 71 percent / lithium aluminium hydride / tetrahydrofuran / 0.17 h / Ambient temperature 5: 75 percent / p-TsOH*H2O / dioxane; H2O / 1.25 h / Heating 6: 47 percent / KOH / aq. ethanol / 0.58 h / Heating View Scheme

oxygen; triethylamine in toluene T=90°C; 4 h; Green chemistry; chemoselective reaction;

oxygen; triethylamine in toluene T=90°C; 4 h; Green chemistry; chemoselective reaction;

N-iodo-succinimide; potassium carbonate in ethyl acetate T=20°C; Inert atmosphereMolecular sieve;