反应条件
1.1: 1.74 g / pyridinium chlorochromate; molecular sieves 4 Angstroem; Celite / CH2Cl2 / 1.5 h / 20 °C
2.1: pyridinium p-toluenesulfonate; MgSO4 / diethyl ether / 18 h / 20 °C
3.1: 52 percent / BF3*Et2O / diethyl ether / 3 h / -78 - -50 °C
4.1: Mg; 1,2-dibromoethane / tetrahydrofuran / 3 h / Heating
4.2: CuBr*Me2S; trimethylsilylchloride / tetrahydrofuran / 1.67 h / -78 °C
4.3: 6.9 g / tetrahydrofuran / 1 h / -78 °C
5.1: diisobutylaluminum hydride / hexane; tetrahydrofuran / 0.75 h / -78 °C
6.1: pyridinium p-toluenesulfonate / 1 h / 20 °C
7.1: 4.4 g / BF3*Et2O / CH2Cl2 / 0.5 h / -78 °C
8.1: methanol; pyridinium p-toluenesulfonate / 18 h / Heating
9.1: 1.92 g / triethylamine / CH2Cl2 / 1 h / 20 °C
10.1: hydrochloric acid / 42 h / 60 °C
View Scheme
参考文献
DeGoey, David A.; Chen, Hui-Ju; Flosi, William J.; Grampovnik, David J.; Yeung, Clinton M.; Klein, Larry L.; Kempf, Dale J.
Journal of Organic Chemistry, 2002 , vol. 67, # 16 p. 5445 - 5453