Multi-step reaction with 10 steps
1.1: mercury(II) diacetate / 36 h / Reflux
2.1: methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide) / dichloromethane / 0.25 h / -78 °C
3.1: n-butyllithium / tetrahydrofuran
3.2: 2 h / -78 °C
4.1: Dess-Martin periodane / dichloromethane / 1 h / 0 °C
5.1: borane-THF; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran / 6 h / -40 °C
6.1: sodium bis(2-methoxyethoxy)aluminium dihydride / 4 h / 40 °C
6.2: 12 h / -78 - 0 °C
7.1: 2,6-dimethylpyridine / dichloromethane / 0.17 h / 20 °C
8.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine / water; acetonitrile / 1.5 h / 80 °C
9.1: pyridine; pyridine hydrogenfluoride / tetrahydrofuran / 3 h / 40 °C
10.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / 1 h / 0 °C
With
pyridine; 2,6-dimethylpyridine; n-butyllithium; tetrapropylammonium perruthennate; borane-THF; mercury(II) diacetate; palladium diacetate; Dess-Martin periodane; pyridine hydrogenfluoride; 4-methylmorpholine N-oxide; methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide); triethylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; tris-(o-tolyl)phosphine; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole;
In
tetrahydrofuran; dichloromethane; water; acetonitrile;
2.1: Claisen rearrangement / 8.1: Heck reaction;
DOI:10.1016/j.tetlet.2011.10.151