Stereoselective Palladium(0)-Mediated Synthesis of Unsaturated 1,4-Disaccharides
摘要:
Unsaturated 1,4-disaccharides are obtained in quite good yields by alkylation of ethyl alpha-O-Delta(2)-glycosides, having a leaving group at C-4, with various 1-hydroxycarbohydrates in the presence of a catalytic amount of palladium(0). The reaction is regio- and stereospecific for alpha-erythro enosides 3 and 5, and only stereospecific in the case of the beta-threo enoside 7, alkylation occurring at C-4 and C-2 in this case.
Stereoselective Palladium(0)-Mediated Synthesis of Unsaturated 1,4-Disaccharides
摘要:
Unsaturated 1,4-disaccharides are obtained in quite good yields by alkylation of ethyl alpha-O-Delta(2)-glycosides, having a leaving group at C-4, with various 1-hydroxycarbohydrates in the presence of a catalytic amount of palladium(0). The reaction is regio- and stereospecific for alpha-erythro enosides 3 and 5, and only stereospecific in the case of the beta-threo enoside 7, alkylation occurring at C-4 and C-2 in this case.
Unsaturated 1,4-disaccharides are obtained in fairly good yields by alkylation of ethyl alpha-O-Delta(2)-glycosides which have a leaving group at the position 4 with various carbohg drates havillg a free anomeric hydroxyl group in the presence of a catalytic amount of palladium(0).