反应条件
1: 95 percent / CH2Cl2 / 15 h / -45 °C 2: 63 percent / Burgess' reagent 3: 100 percent / pyridine 4: 65 percent / OsO4 5: DBU / toluene / 2 h / 105 °C 6: 75 percent / pyridine, DMAP / 24 h / 25 °C 7: 100 percent / HF*pyridine / acetonitrile / 11 h / 0 °C 8: tetrahydrofuran / 0.17 h / -78 °C 9: tetrapropylammonium perruthenate, NMO, molecular sieves / CH2Cl2 / 0.25 h / 25 °C 10: 1.) t-BuOK, 2.) benzeneseleninic anhydride, 3.) t-BuOK 11: pyridine, DMAP / 20 h / 25 °C 12: 94 percent / TASF / tetrahydrofuran / 1 h / 25 °C 13: 1.) LHMDS / 1.) THF, 2.) THF, 0 deg C, 1 h 14: HF, pyridine / acetonitrile / 1 h / 0 °C 15: H2 / Pd/C / ethanol / 1 h View Scheme
参考文献
Holton; Kim; Somoza; Liang; Biediger; Boatman; Shindo; Smith; Nadizadeh; Suzuki; Tao; Vu; Tang; Zhang; Murthi; Gentile; Liu
Journal of the American Chemical Society, 1994 , vol. 116, # 4 p. 1599 - 1600