反应条件
1: 99 percent / 4-methylmorpholine N-oxide / OsO4 / 2-methyl-propan-2-ol; tetrahydrofuran; H2O / 18 h / 20 °C 2: 98 percent / lead tetraacetate / benzene / 2 h / 20 °C 3: 1.06 g / diisopropylamine; n-BuLi / tetrahydrofuran; hexane / 3 h / -78 °C 4: 820 mg / N-methylmorpholine N-oxide / OsO4 / 2-methyl-propan-2-ol; tetrahydrofuran; H2O / 24 h / 20 °C 5: H5IO6 / tetrahydrofuran; H2O / 3 h / 20 °C 6: 732 mg / methanol; benzene; hexane / 15 h / 20 °C 7: 91 percent / lithium; t-BuOH / liquid ammonia; tetrahydrofuran / 2 h / -78 °C 8: 90 percent / CrO3; pyridine / CH2Cl2 / 0.5 h / 20 °C 9: 82 percent / SmI2; methanol / tetrahydrofuran / 2 h 10: 24 percent / imidazole; DMAP / dimethylformamide / 22 h / 20 °C 11: 92 percent / N-methylmorpholine N-oxide / TPAP / CH2Cl2 / 0.5 h / 20 °C 12: 76 percent / NaOMe / methanol / 12 h / 20 °C 13: 99 percent / tetrahydrofuran; diethyl ether / 1.5 h / 20 °C 14: 95 percent / TBAF / tetrahydrofuran / 3 h 15: 61 percent / p-toluenesulfonic acid / benzene / 48 h / 60 °C 16: 76 percent / CuBr2 / acetonitrile / 72 h / 50 °C 17: 71 percent / Li2CO3; LiBr / dimethylformamide / 17 h / 140 °C View Scheme
参考文献
Marcos; Cubillo; Moro; Carballares; Diez; Basabe; Llamazares; Beneitez; Sanz; Broughton; Urones
Tetrahedron, 2005 , vol. 61, # 4 p. 977 - 1003
