Multi-step reaction with 7 steps
1.1: NaH / dimethylformamide / 48 h / 20 °C
1.2: 103 mg / TBAF / tetrahydrofuran / 20 °C
2.1: n-BuLi; c-C5H9MgCl / Ti(OiPr)3Cl / toluene; hexane; diethyl ether / 1 h / -40 °C
2.2: BF3*OEt2 / toluene; hexane; diethyl ether / 1 h / -78 °C
2.3: 232 mg / DDQ / CH2Cl2 / 0.33 h / 0 °C
3.1: 92 percent / 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one / CH2Cl2 / 1.5 h / 0 - 20 °C
4.1: 92 percent / DIBAL / hexane; CH2Cl2 / 0.17 h / -78 °C
5.1: 95 percent / 2,6-lutidine / CH2Cl2 / 1 h / 0 °C
6.1: 99 percent / DIBAL / toluene; hexane / -78 - 0 °C
7.1: 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-2-one / CH2Cl2 / 1.5 h / 0 - 20 °C
With
2,6-dimethylpyridine; n-butyllithium; sodium hydride; diisobutylaluminium hydride; cyclopentylmagnesium chloride; Dess-Martin periodane;
triisopropoxytitanium(IV) chloride;
In
diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; toluene;
3.1: Dess-Martin oxidation / 7.1: Dess-Martin oxidation;
DOI:10.1021/ol0600786