Multi-step reaction with 12 steps
1.1: OsO4; K3Fe(CN)6; 1,4-diazabicyclo[2.2.2]octane / K2CO3; NaHCO3 / H2O; 2-methyl-propan-2-ol
2.1: NaIO4 / tetrahydrofuran; H2O
3.1: 94 percent / Me4NBH(OAc)3 / acetic acid; acetonitrile / 10 h / -20 °C
4.1: camphorsulfonic acid / 16 h / 20 °C
5.1: HF*pyridine / tetrahydrofuran
6.1: (COCl)2; DMSO; triethylamine / CH2Cl2 / -78 °C
7.1: SmI2 / tetrahydrofuran / 20 °C
8.1: DMSO; (CF3CO)2O / CH2Cl2 / -78 °C
8.2: 88 percent / acetylacetone; triethylamine / CH2Cl2 / -60 - -40 °C
9.1: camphorsulfonic acid / 1.5 h / 20 °C
10.1: 90 percent / CaSO4; Ag2O / 72 h
11.1: 92 percent / tetrabutylammonium fluoride / tetrahydrofuran / 2 h / 0 °C
12.1: 95 percent / Dess-Martin periodinane / CH2Cl2 / 1 h
With
1,4-diaza-bicyclo[2.2.2]octane; calcium sulfate; sodium periodate; osmium(VIII) oxide; samarium diiodide; oxalyl dichloride; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; Dess-Martin periodane; pyridine hydrogenfluoride; dimethyl sulfoxide; triethylamine; trifluoroacetic anhydride; silver(l) oxide; tetramethylammonium triacetoxyborohydride; potassium hexacyanoferrate(III);
sodium hydrogencarbonate; potassium carbonate;
In
tetrahydrofuran; dichloromethane; water; acetic acid; acetonitrile; tert-butyl alcohol;
7.1: Barbier coupling / 12.1: Dess-Martin oxidation;
DOI:10.1002/anie.200390322