反应条件
1: 64 percent / m-chloroperbenzoic acid, lithium carbonate, 4,4'-thiobis(2-tert-butyl-6-methylphenol) / CH2Cl2 / 168 h / Heating
2: 100 percent / aq. sodium hydroxide / tetrahydrofuran / 1 h
3: 94 percent / diborane / tetrahydrofuran / 1) -20 deg C, 3 h; 2) -10 deg C, 3 h; 3) 0 deg C, 3 h; 4) 25 deg C, 4.5 h
4: 76 percent / imidazole / dimethylformamide / 18 h / Ambient temperature
5: 46 percent / thionyl chloride, pyridine / benzene / 0.42 h / Ambient temperature
6: 1.) lithium diisopropylamide / 1) THF, hexane, -78 deg C, 10 min, -25 deg C, 10 min; 2) -23 deg C, 10 min
7: pyridine / CH2Cl2 / 4.5 h / Ambient temperature
8: 77 percent / 1,5-diazobicyclo<5.4.0>undec-5-ene / benzene / 0.67 h
9: 67 percent / Dowex 50W-X8 (H+) / CHCl3 / 3 h
10: 5.0 mg / pyridine, 4-dimethylaminopyridine / tetrahydrofuran / 43 h
11: 81 percent / Dowex 1-X8 (OH(1-)), methanol / 2 h / 0 °C
View Scheme
参考文献
Grieco; Oguri; Gilman
Journal of the American Chemical Society, 1980 , vol. 102, # 18 p. 5886 - 5891