2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide reacted with carboxylic acids in the presence of CaH_2 and Ag_2CO_3 and small amount of I_2 to give good yields of l-O-acyl-β-D- galactopyranose tetraaeetates.β-A...2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide reacted with carboxylic acids in the presence of CaH_2 and Ag_2CO_3 and small amount of I_2 to give good yields of l-O-acyl-β-D- galactopyranose tetraaeetates.β-Anomers of glycosyl esters were obtained by this improved Koenigs-Knorr method.展开更多
文摘2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide reacted with carboxylic acids in the presence of CaH_2 and Ag_2CO_3 and small amount of I_2 to give good yields of l-O-acyl-β-D- galactopyranose tetraaeetates.β-Anomers of glycosyl esters were obtained by this improved Koenigs-Knorr method.
