1: 1.1 g / H2, glacial acetic acid / 10percent palladium-on-charcoal / methanol / 24 h / 2250.2 Torr 2: 100 percent / glacial acetic acid / H2O / 8 h / 60 °C View Scheme

Multi-step reaction with 5 steps 1: 1.) dibutyltin oxide, 2.) tetrabutylammonium bromide / 1.) toluene, reflux 2.) toluene, 100 deg C, 8 h2: 95 percent / pyridine / CH2Cl2 / 1 h3: 10.6 g / lithium azide / CH2Cl2; dimethylformamide / 8 h / -40 °C4: NiCl2, NaBH4 / ethanol / 0 °C5: 9.6 g / pyridine / 2 h / 40 °C  

Multi-step reaction with 6 steps 1: 75 percent / N-methylmorpholine N-oxide hydrate, OsO4 / acetone; H2O; 2-methyl-propan-2-ol2: 1.) dibutyltin oxide, 2.) tetrabutylammonium bromide / 1.) toluene, reflux 2.) toluene, 100 deg C, 8 h3: 95 percent / pyridine / CH2Cl2 / 1 h4: 10.6 g / lithium azide / CH2Cl2; dimethylformamide / 8 h / -40 °C5: NiCl2, NaBH4 / ethanol / 0 °C6: 9.6 g / pyridine / 2 h / 40 °C  

Multi-step reaction with 4 steps 1: 95 percent / pyridine / CH2Cl2 / 1 h2: 10.6 g / lithium azide / CH2Cl2; dimethylformamide / 8 h / -40 °C3: NiCl2, NaBH4 / ethanol / 0 °C4: 9.6 g / pyridine / 2 h / 40 °C  

Multi-step reaction with 2 steps 1: NiCl2, NaBH4 / ethanol / 0 °C2: 9.6 g / pyridine / 2 h / 40 °C  

Multi-step reaction with 7 steps 1: 70 percent / NaI, Zn / dimethylformamide / 3 h / 135 °C2: 75 percent / N-methylmorpholine N-oxide hydrate, OsO4 / acetone; H2O; 2-methyl-propan-2-ol3: 1.) dibutyltin oxide, 2.) tetrabutylammonium bromide / 1.) toluene, reflux 2.) toluene, 100 deg C, 8 h4: 95 percent / pyridine / CH2Cl2 / 1 h5: 10.6 g / lithium azide / CH2Cl2; dimethylformamide / 8 h / -40 °C6: NiCl2, NaBH4 / ethanol / 0 °C7: 9.6 g / pyridine / 2 h / 40 °C  

Multi-step reaction with 3 steps 1: 10.6 g / lithium azide / CH2Cl2; dimethylformamide / 8 h / -40 °C2: NiCl2, NaBH4 / ethanol / 0 °C3: 9.6 g / pyridine / 2 h / 40 °C  

With  hydrogen; acetic acid; palladium on activated charcoal in  methanol P=2250.2 Torr; 24 h;