反应条件
1.1: (-)-B-methoxydiisopinocampheylborane / diethyl ether / 1.25 h / -78 - 20 °C 1.2: diethyl ether / -78 - 20 °C / Acid hydrolysis 1.3: 76 percent / aq. NaOH; aq. H2O2 / 3 h / Heating 2.1: 99 percent / Et3N; DMAP / CH2Cl2 / 1.5 h / 20 °C 3.1: 87 percent / NaN3 / dimethylformamide / 2 h / 80 °C 4.1: Ph3P / tetrahydrofuran 4.2: 66 percent / H2O 5.1: 89 percent / Et3N; DMAP / CH2Cl2 / 4.5 h / 0 - 20 °C 6.1: 79 percent / Cl2Ru(CHPh)(PCy3)2 / CH2Cl2 / 12 h / Heating 7.1: 98 percent / NaOH / tetrahydrofuran / 2 h / 20 °C 8.1: 67 percent / Et3N; DMAP / CH2Cl2 / 1.5 h / 20 °C 9.1: 89 percent / NaH / tetrahydrofuran / 0 - 20 °C 10.1: 50 percent / DDQ / dioxane / 4 h / 110 °C 11.1: 78 percent / HCl / tetrahydrofuran / 3 h / Heating View Scheme
参考文献
Danieli, Bruno; Lesma, Giordano; Passarella, Daniele; Sacchetti, Alessandro; Silvani, Alessandra; Virdis, Andrea
Organic Letters, 2004 , vol. 6, # 4 p. 493 - 496