The first partial syntheses of galactosyl-glucosyl oleanolic acid disacchar
ides are described. Arvensoside B and calenduloside A, which have earlier b
een isolated from Calendula arvensis and Calendula officinalis, and some fu
rther oleanolic acid glycosides were prepared from differently linked aceto
bromo sugars. The hemolytic properties of these saponins were investigated.
Systematic variation of the carbohydrate structure and comparison with alr
eady synthesized glucosyl-glucosyl analogues enable general conclusions abo
ut structure-activity relationships.