反应条件
1.1: 96 percent / TEA / CH2Cl2
2.1: 92 percent / NBS / tetrahydrofuran / 20 °C
3.1: DIBAL-H / CH2Cl2 / -78 °C
4.1: LHMDS / tetrahydrofuran / 0.5 h / 0 °C
4.2: 368 mg / tetrahydrofuran / 20 °C
5.1: DIBAL-H / CH2Cl2 / 2 h / -78 °C
6.1: 910 mg / imidazole / CH2Cl2 / 2 h / Heating
7.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C
7.2: tetrahydrofuran; hexane / 1 h / -78 °C
8.1: 98 mg / aq. oxalic acid / tetrahydrofuran / 0.17 h
9.1: toluene / 3.5 h / 110 °C
9.2: 64 percent / air / toluene / 2 h / 20 °C
10.1: 65 percent / 4A molecular sieves; TBAF / tetrahydrofuran / 0.5 h / 0 °C
View Scheme
参考文献
Trost, Barry M.; Thiel, Oliver R.; Tsui, Hon-Chung
Journal of the American Chemical Society, 2003 , vol. 125, # 43 p. 13155 - 13164