反应条件
1.1: ozone / methanol / 0.5 h / -78 °C 1.2: Me2S / methanol / 5 h / -78 - 20 °C 2.1: NaH2PO4; 2-methyl-2-butene; sodium chlorite / 2-methyl-propan-2-ol / 2 h / 20 °C 3.1: 134 mg / H2SO4 / ethanol / 9 h / 80 °C 4.1: 40 percent / isopropylmagnesium bromide / tetrahydrofuran / 11 h / 4 °C 5.1: 4-(dimethylamino)pyridine; pyridine / 2 h / 20 °C 6.1: 3.1 g / triethylamine; 4-(dimethylamino)pyridine / CH2Cl2 / 11 h / 20 °C 7.1: LHMDS / tetrahydrofuran / 0.5 h / -78 °C 8.1: 1.93 g / NaHCO3; H2O2 / tetrahydrofuran; ethyl acetate / 0.5 h / 20 °C 9.1: (diethylamino)diphenylsilyllithium; diethyl zinc / tetrahydrofuran; hexane / -78 °C 9.2: 57 percent / m-chloroperoxybenzoic acid; KHF2 / dimethylformamide / 2 h / 20 °C 10.1: 58 percent / BuLi; HMPA; diisopropylamine / hexane; tetrahydrofuran / 4 h / -78 °C 11.1: 355 mg / trifluoroacetic acid / CH2Cl2 / 3 h / 20 °C 12.1: NaOH / H2O / 64 h / 4 °C 13.1: 149 mg / triethylamine; bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH2Cl2 / 2 h / 20 °C View Scheme
参考文献
Fukuda, Nobuhisa; Sasaki, Kazuki; Sastry; Kanai, Motomu; Shibasaki, Masakatsu
Journal of Organic Chemistry, 2006 , vol. 71, # 3 p. 1220 - 1225