Multi-step reaction with 14 steps
1.1: CF3SO3H / diethyl ether / 0.17 h / 0 °C
2.1: 371 mg / TBAF / tetrahydrofuran / 1 h / 20 °C
3.1: 91 percent / pyridine; DMAP / 3 h / 25 °C
4.1: OsO4; aq. NMO / acetone / 12 h / 20 °C
5.1: 3.2 g / aq. NaIO4 / tetrahydrofuran / 0 °C / pH 7
6.1: 94 percent / BF3*Et2O / CH2Cl2 / 2 h / -78 °C
7.1: 2,6-lutidine / CH2Cl2 / -50 °C
8.1: 347 mg / DIBALH / toluene; hexane / 2 h / -78 °C
9.1: DMSO; (COCl)2; Et3N / CH2Cl2 / 1.5 h / -70 - -30 °C
10.1: NaHMDS / tetrahydrofuran / 0.17 h / 0 °C
10.2: 309 mg / tetrahydrofuran / 1 h / -78 °C
11.1: 89 percent / DIBAL-H / toluene; hexane / 2 h / -78 °C
12.1: 98 percent / L-(+)-diethyl tartrate; Ti(i-OPr)4; t-BuOOH / 4 Angstroem molecular sieves / CH2Cl2; decane / 14.5 h / -25 - -20 °C
13.1: 86 percent / TBAF / tetrahydrofuran / 1.5 h / 0 °C
14.1: 76 percent / Ti(O-iPr)4 / benzene / 2 h / Heating
With
pyridine; 2,6-dimethylpyridine; titanium(IV) isopropylate; tert.-butylhydroperoxide; dmap; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; oxalyl dichloride; diethyl (2R,3R)-tartrate; trifluorormethanesulfonic acid; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine;
4 A molecular sieve;
In
tetrahydrofuran; diethyl ether; decane; hexane; dichloromethane; acetone; toluene; benzene;
10.2: Wadsworth-Emmons olefination / 12.1: Sharpless reaction;
DOI:10.1039/b308305e