Guo_2009_Carbohydr.Res_344_1167

Reference

Title : Facile synthesis of three bidesmosidic oleanolic acid saponins with strong inhibitory activity on pancreatic lipase - Guo_2009_Carbohydr.Res_344_1167
Author(s) : Guo T , Liu Q , Wang P , Zhang L , Zhang W , Li Y
Ref : Carbohydr Res , 344 :1167 , 2009
Abstract :

The first synthesis of scabiosaponins E (1), F (2), and G (3), three new oleanolic acid saponins with strong inhibitory activity on pancreatic lipase isolated from the Chinese traditional medicinal herb Scabiosa tschiliensis, was efficiently achieved in an one-pot strategy under the combined use of glycosyl trichloroacetimidates and p-toluene 1-thioglycosides (STol) as donors.

PubMedSearch : Guo_2009_Carbohydr.Res_344_1167
PubMedID: 19463989

Related information

Inhibitor Oleanolic-acid

Citations formats

Guo T, Liu Q, Wang P, Zhang L, Zhang W, Li Y (2009)
Facile synthesis of three bidesmosidic oleanolic acid saponins with strong inhibitory activity on pancreatic lipase
Carbohydr Res 344 :1167

Guo T, Liu Q, Wang P, Zhang L, Zhang W, Li Y (2009)
Carbohydr Res 344 :1167