5-O-苯甲酰基-1,2-二-O-乙酰基-3-脱氧-D-呋喃核糖合成路线 (共 5 条)
反应条件
1: [(3aR,5S,6aR)-2,2-dimethyltetrhydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate With acetic acid 2 h; Heating; 2: acetic anhydride With pyridine; 4-(N,N-dimethlyamino)pyridine T=20°C; Further stages.;
参考文献
Zlatev, Ivan; Vasseur, Jean-Jacques; Morvan, Francois
Tetrahedron Letters, 2008 , vol. 49, # 20 p. 3288 - 3290
反应条件
1: 93 percent / SnCl4 / acetonitrile 2: 94 percent / K2CO3, MeOH / Heating 3: 81 percent / pyridine 4: 66 percent / iPr2NEt / tetrahydrofuran View Scheme
参考文献
Rizzo; Dougherty; Breslow
Tetrahedron Letters, 1992 , vol. 33, # 29 p. 4129 - 4132
反应条件
tin(IV) chloride in acetonitrile
参考文献
Rizzo; Dougherty; Breslow
Tetrahedron Letters, 1992 , vol. 33, # 29 p. 4129 - 4132
反应条件
1: With benzenesulfonamide in acetonitrile
1 h; Heating;
2: With trimethylsilyl trifluoromethanesulfonate
T=20°C; 5 h;
3: With ammonium hydroxide in tetrahydrofuran; methanol
T=50°C; 6 h; Further stages.;
参考文献
Zlatev, Ivan; Vasseur, Jean-Jacques; Morvan, Francois
Tetrahedron Letters, 2008 , vol. 49, # 20 p. 3288 - 3290
反应条件
1: 62 percent / SnCl4 / 1,2-dichloro-ethane / 20 h / 27 °C
2: 98 percent / NH3 / methanol / 12 h / 25 °C
View Scheme
参考文献
Sheppard, Terry L.; Rosenblatt, Andrew T.; Breslow, Ronald
Journal of Organic Chemistry, 1994 , vol. 59, # 24 p. 7243 - 7248