反应条件
1: diisobutylaluminum hydride (DIBAL) / CH2Cl2; hexane / 0.5 h / -78 °C
2: 1 M aq. HCl / diethyl ether / 1 h
3: 1.) t-BuLi, 2.) dineopentylzinc
4: (CH3)2SO, pyridine, CF3COOH, dicyclohexylcarbodiimide (DCC) / benzene / 0.5 h / Ambient temperature
5: benzene; diethyl ether / 0.33 h
6: n-Bu4NF / tetrahydrofuran / 0.25 h / 0 °C
7: 75percent aq. CH3COOH / tetrahydrofuran / 0 - 5 °C
8: 68 percent / diethyl cyanophosphonate, Et3N / dimethylformamide / 0.5 h / 0 °C
9: 86 percent / (COCl)2, (CH3)2SO / CH2Cl2 / 0.33 h / -78 °C
10: 69 percent / lithium bis(trimethylsilyl)amide / tetrahydrofuran / 2.5 h / 0 °C
11: 100 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), H2O / CH2Cl2 / 0.5 h / Ambient temperature
12: 64 percent / CF3COOH / 2.5 h / Ambient temperature
View Scheme
参考文献
Smith III; Rano; Chida; Sulikowski; Wood
Journal of the American Chemical Society, 1992 , vol. 114, # 21 p. 8008 - 8022