1,2-o-异亚丙基-3-苄氧基-d-呋喃葡萄糖合成路线 （共 31 条）
反应条件
acetic acid T=70°C; 3 h;
参考文献
Arun; Joshi; Puranik; Bhawal; Deshmukh
Tetrahedron, 2003 , vol. 59, # 13 p. 2309 - 2316
反应条件
(3a,9R,3'''a,4'"b,9'"R)-9,9'-[1,4-phthalazinediylbis(oxy)]bis[6'-(methyloxy)-10,11-dihydrocinchonan]; N-methyl-2-indolinone; polysulfone microencapsulated OsO4 in water; acetone; acetonitrile T=20°C; 0.416667 h;
参考文献
Malla Reddy; Srinivasulu; Venkat Reddy; Narasimhulu; Venkateswarlu
Tetrahedron Letters, 2006 , vol. 47, # 30 p. 5285 - 5288
反应条件
12-molybdophosphoric acid HPMo; silica gel in dichloromethane T=20°C; 3 h; chemoselective reaction;
参考文献
Kumar, Ponminor Senthil; Kumar, Gaddale Devanna Kishore; Baskaran, Sundarababu
European Journal of Organic Chemistry, 2008 , # 36 p. 6063 - 6067
反应条件
2,3-dicyano-5,6-dichloro-p-benzoquinone in dichloromethane; water T=20°C; 4 h;
参考文献
Vatele, Jean-Michel
Tetrahedron, 2002 , vol. 58, # 28 p. 5689 - 5698
反应条件
1: With lithium aluminium tetrahydride in tetrahydrofuran T=70°C; 2 h; 2: With water in tetrahydrofuran; acetone
参考文献
Kapeller, Dagmar C.; Hammerschmidt, Friedrich
Tetrahedron, 2010 , vol. 66, # 3 p. 591 - 598
反应条件
1: NaH; tetrabutylammonium iodide / tetrahydrofuran / 14 h / 20 °C 2: 17.8 g / acetic acid / H2O / 16 h / 20 °C View Scheme
参考文献
Journal of Organic Chemistry, , vol. 68, # 19 p. 7559 - 7561
反应条件
1: NaH; tetrabutylammonium iodide / tetrahydrofuran / 14 h / 20 °C 2: 17.8 g / acetic acid / H2O / 16 h / 20 °C View Scheme
参考文献
Journal of Organic Chemistry, , vol. 68, # 19 p. 7559 - 7561
反应条件
methanol T=20°C; 3 h;
参考文献
Kapeller, Dagmar C.; Hammerschmidt, Friedrich
Tetrahedron, 2010 , vol. 66, # 3 p. 591 - 598
反应条件
1: 95 percent / NaH / tetrahydrofuran; dimethylsulfoxide / 3 h / Heating 2: 60percent acetic acid / 16 h / Ambient temperature View Scheme
参考文献
Journal of Organic Chemistry, , vol. 46, # 7 p. 1296 - 1309
反应条件
AD-mix-α in water; tert-butyl alcohol T=0°C; Sharpless asymmetric dihydroxylation; 96 h; Title compound not separated from byproducts;
参考文献
Journal of Carbohydrate Chemistry, , vol. 19, # 9 p. 1201 - 1210
