反应条件
1: 63.9 percent / m-Chloroperbenzoic acid / acetic acid
2: Ammonium sulfate / pyridine / 4 h / Heating
3: SnCl4 / acetonitrile / 18 h / Ambient temperature
4: 65 percent / POCl3, 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose / Molecular sieve 4A / CHCl3 / 24 h / 30 - 33 °C
5: 35 mg / Conc. HCl / ethanol / 4 h
View Scheme
参考文献
Itoh; Ono; Sugawara; Mizuno
Journal of Heterocyclic Chemistry, 1982 , vol. 19, # 3 p. 513 - 517