反应条件
1: NaH / tetrahydrofuran / 1.) reflux, 1 h, 2.) r.t., 1 h
2: 1.) CuI / 1.) ether, -20 deg C, 10 min, 2.) ether, -78 deg C, 0.5 h; -20 deg C, 15 h
3: 94 percent / DIBAL / toluene / 1 h / -78 °C
4: 99 percent / pyridine, DMAP / 0.5 h / 0 °C
5: 1.) n-BuLi, Me3SnCl, 2.) LiCl / 2.) Pd(dba)2 / 1.) THF, hexane, -50 deg C, 0.5 h; -50 deg C, 3 h, 2.) DMF, 100 deg C, 4 h
6: 71 percent / CrO3, 3,5-dimethylpyrazole / CH2Cl2 / 0.5 h / -20 °C
7: 43 percent / BBr3 / CH2Cl2 / 2.5 h / -78 - -10 °C
8: 62 percent / BF3*Et2O / CH2Cl2 / 1 h / Ambient temperature
9: 67 percent / Raney nickel W-7 / ethanol / 3 h / Heating
10: 87 percent / LiAlH4 / tetrahydrofuran / 1 h / 0 °C
11: 77 percent / aq. potassium nitrosodisulfonate, KH2PO4 / acetone / 0.5 h / Ambient temperature
View Scheme
参考文献
Mori, Kenji
Bulletin des Societes Chimiques Belges, 1992 , vol. 101, # 5 p. 393 - 406