反应条件
1.1: LDA / hexane; tetrahydrofuran / 1 h / -78 °C 1.2: hexane; tetrahydrofuran / -78 - 20 °C 2.1: 897 mg / Pd(OAc)2 / acetonitrile / 1 h / Heating 3.1: LiHMDS / tetrahydrofuran; hexane / 0.5 h / -78 - 0 °C 3.2: 91 percent / tetrahydrofuran; hexane / 1.5 h / -78 - 50 °C 4.1: 96 percent / hydrogen / Pd/C / ethanol / 4 h / 20 °C / 760 Torr 5.1: NaH / dimethylsulfoxide / 1 h / 0 - 20 °C 5.2: 91 percent / dimethylsulfoxide / 24 h / 75 - 80 °C 6.1: 81 percent / hydrogen; MeOH / Pd/C / triethylamine / 12 h / 20 °C / 760 Torr 7.1: 100 percent / aq. HCl / tetrahydrofuran / 2 h / 20 °C 8.1: n-BuLi / dioxane; hexane / 1 h / 20 °C 8.2: 93 percent / dioxane; hexane / 4 h / 110 °C 9.1: 54 percent / ammonium cerium(IV) nitrate / acetonitrile; H2O / 11 h / -7 - 20 °C / pH 0.7 - 1.3 View Scheme
参考文献
Poigny, Stephane; Guyot, Michele; Samedi, Mohammad
Journal of Organic Chemistry, 1998 , vol. 63, # 17 p. 5890 - 5894