反应条件
1: NaOEt / ethanol; tetrahydrofuran / a) -15 deg C, 3 h, b) 4 deg C, 12 h
2: xylene / 3 h / Heating
3: 93 percent / KOH / ethanol / 1.5 h / Heating
4: 73 percent / copper chromite / quinoline / 3 h / 230 °C
5: acetic acid / CH2Cl2 / 2 h / Ambient temperature
6: 1.) iodomethane / 1.) THF, from 0 deg C to 4 deg C, 30 h, 2.) water, 80 deg C, 3.5 h
7: H2, NH3 / Raney nickel / ethanol / 48 h / 2508 Torr / Ambient temperature
8: 1.) NaOEt / 1.) ethanol, 0 deg C, 1 h, 2.) ethanol, RT, 3 h
9: H2 / 10percent Pd/C / ethanol / 48 h / 2508 Torr / Ambient temperature
10: Fremy's salt, aq. KH2PO4 / acetone / 4 h / 0 °C
11: 1.) t-BuOK / 1.) THF, 0 deg C, 1 h, 2.) THF, RT, 3 h
12: p-toluenesulfonic acid / acetonitrile / 5 h / Ambient temperature
13: NaHCO3 / ethanol / 3 h / Heating
14: CH2Cl2 / 3 h / Ambient temperature
15: PhI(OCOCF3)2 (PIFA) / various solvent(s) / 0.33 h / Ambient temperature
View Scheme
参考文献
Kita, Yasuyuki; Tohma, Hirofumi; Inagaki, Masanao; Hatanaka, Kenji; Yakura, Takayuki
Journal of the American Chemical Society, 1992 , vol. 114, # 6 p. 2175 - 2180