反应条件
1: NaIO4 / 24 h / Ambient temperature 2: p-TsOH / benzene / 24 h / Heating 3: 80 percent / mCPBA / CH2Cl2 / 24 h / -20 - 0 °C 4: iPr2NEt / CH2Cl2 / 0.5 h / -78 °C 5: 1) mCPBA, KHCO3, 2) citric acid / 1) CH2Cl2, -30 to -20 deg C, 1 h, 2) MeOH, 0 deg C to RT 6: NaIO4 / methanol; H2O / 0 deg C, 12 h; RT, 3 h 7: CHCl3 / Ambient temperature 8: 71 percent / LTBA / tetrahydrofuran / -78 to -40 deg C; -35 deg C, 4 h 9: 89 percent / nBu3P / tetrahydrofuran / 1 h / 0 - 20 °C 10: 85 percent / 30percent H2O2 / tetrahydrofuran / 18 h / 0 - 20 °C 11: I2, NaHCO3 / CH2Cl2 / 48 h / Ambient temperature 12: 90 percent / methanol / 4 h / 0 - 20 °C 13: LTBA / tetrahydrofuran / 3 h / 0 °C 14: pyridine / 2 h / 0 - 20 °C 15: 56 percent / CSA, dihydroquinone / benzene / 3 h / Heating 16: 1) mCPBA, 2) 2N HCl / 1) CH2Cl2, -30 to -25 deg C, 20 h, 2) THF, RT, 16 h 17: Me4NBH(OAc)3 / acetic acid; acetonitrile / 2 h / 0 °C 18: DDQ / dioxane / 4 h / 80 °C 19: 94 percent / Ag2O / acetonitrile / 24 h / Ambient temperature 20: 92 percent / MsCl, Et3N / CH2Cl2 / Ambient temperature 21: 47 percent / OsO4, DABCO / tetrahydrofuran / 24 h / -40 °C 22: 92 percent / pyridinium p-toluenesulfonate / CH2Cl2 / 16 h / Ambient temperature 23: CH(NMe2)3 / 1 h / 100 °C 24: 2N HCl / tetrahydrofuran / 20 h / Ambient temperature 25: PCC / CH2Cl2 / 5 h / Ambient temperature 26: CH2Cl2 / 0.33 h / Ambient temperature 27: DBN / CH2Cl2 / 6 h / Ambient temperature 28: K2CO3, MeOH / 5 h / Ambient temperature 29: 1N HCl / tetrahydrofuran / 12 h / Ambient temperature 30: 49 percent / pyridine / 12 h / -20 °C 31: 73 percent / PCC / CH2Cl2 / 2 h / Ambient temperature View Scheme
参考文献
Sato, Seiji; Nakada, Masahisa; Shibasaki, Masakatsu
Tetrahedron Letters, 1996 , vol. 37, # 34 p. 6141 - 6144
