反应条件
1: acetic acid; methanol / 2 h / 200 °C
2: magnesium sulfate / CH2Cl2 / 0.02 h / 20 °C
3: 63 percent / benzene / 0.17 h / Heating
4: 66 percent / bis(benzonitrile)palladium(II) chloride, air / 2-methyl-propan-2-ol / 116 °C
5: 100 percent / aluminum isopropoxide / propan-2-ol / Heating
6: pyridine / 15 h / 20 °C
7: tetrakis(triphenylphosphine)palladium(0) / tetrahydrofuran / 24 h / 100 °C
8: trifluoroacetic acid / CH2Cl2 / 0.5 h
9: 99 percent / N-methylmorpholine, osmium tetraoxide / tetrahydrofuran; H2O / 24 h / 20 °C
10: 1.) methyl sulfide, N-chlorosuccinimide, 2.) triethylamine / 1.) dichloromethane, -40 deg C, 1 h, 2.) from -40 to 20 deg C, 1.5 h
11: 97 percent / trifluoromethanesulfonic acid / CH2Cl2 / 24 h
12: 88 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / Heating
View Scheme
参考文献
Kuehne; Bornmann; Parsons; Spitzer; Blount; Zubieta
Journal of Organic Chemistry, 1988 , vol. 53, # 15 p. 3439 - 3450