2,3,4,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSYL CHLORIDE合成路线 (共 18 条)
反应条件
1: sodium azide / water; acetone / 20 °C 2: palladium 10 on activated carbon; hydrogen / dichloromethane View Scheme
参考文献
Srivastava, Amrita; Varghese, Babu; Loganathan, Duraikkannu
Chemistry - A European Journal, 2013 , vol. 19, # 52 p. 17720 - 17732
反应条件
pyridine; benzyl alcohol zinc salt 1.) CH2Cl2, reflux, 24 h, 2.) room temperature, 24 h; Multistep reaction. Yields of byproduct given;
参考文献
Carbohydrate Research, , vol. 285, p. 159 - 165
反应条件
pyridine; acetic anhydride 1.) CH2Cl2, reflux, 24 h, 2.) room temperature, 24 h; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Carbohydrate Research, , vol. 285, p. 159 - 165
反应条件
pyridine; benzyl alcohol zinc salt 1.) CH2Cl2, reflux, 24 h, 2.) room temperature, 24 h; Multistep reaction. Yields of byproduct given;
参考文献
Carbohydrate Research, , vol. 285, p. 159 - 165
反应条件
pyridine; acetic anhydride 1.) CH2Cl2, reflux, 24 h, 2.) room temperature, 24 h; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Carbohydrate Research, , vol. 285, p. 159 - 165
反应条件
potassium carbonate 1 h; Neat (no solvent)Ball milling;
参考文献
Ramrao Patil, Premanand; Ravindranathan Kartha
Green Chemistry, 2009 , vol. 11, # 7 p. 953 - 956
反应条件
pyridine; benzyl alcohol zinc salt 1.) CH2Cl2, reflux, 24 h, 2.) room temperature, 24 h; Multistep reaction. Yields of byproduct given;
参考文献
Carbohydrate Research, , vol. 285, p. 159 - 165
反应条件
pyridine; acetic anhydride 1.) CH2Cl2, reflux, 24 h, 2.) room temperature, 24 h; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Carbohydrate Research, , vol. 285, p. 159 - 165
反应条件
tetra-.mu.-acetatodichromium dihydrate; (ethylenedinitrilo)tetraacetic acid disodium salt in water; ethyl acetate pH=5.0; 18 h;
参考文献
Kovacs, Gyoengyver; Micskei, Karoly; Somsak, Laszlo
Carbohydrate Research, 2001 , vol. 336, # 3 p. 225 - 228
反应条件
pyridine; chromium(II) diacetate dimer; ethylenediamine 1.) DMF, 70 deg C, 17 h, 2.) 5 h; Yield given. Multistep reaction;
参考文献
Pollon, J. H. P.; Llewellyn, G.; Williams, J. M.
Synthesis, 1989 , # 10 p. 758 - 759