反应条件
1.1: 23.1 g / sodium borohydride / ethanol / 1.5 h / 0 - 20 °C 2.1: thionyl bromide / CH2Cl2 / 1 h / 20 °C 3.1: 3.79 g / aq. sodium sulfite; tetra-n-butylammonium bromide / acetone / 2 h / Heating 4.1: 12 h / 120 °C 4.2: thionyl chloride / 20 °C 5.1: 166.8 mg / sodium azide / dimethylformamide / 22 h / 70 °C 6.1: 86 percent / lithium aluminum hydride / tetrahydrofuran / -78 - 0 °C View Scheme
参考文献
Michelotti, Enrique L.; Moffett, Kristofer K.; Nguyen, Duyan; Kelly, Martha J.; Shetty, Rupa; Chai, Xiaomei; Northrop, Katrina; Namboodiri, Variketta; Campbell, Brandon; Flynn, Gary A.; Fujimoto, Ted; Hollinger, Frank P.; Bukhtiyarova, Marina; Springman, Eric B.; Karpusas, Michael
Bioorganic and Medicinal Chemistry Letters, 2005 , vol. 15, # 23 p. 5274 - 5279
