A HIGHLY STEREOCONTROLLED SYNTHESIS OF THE PROPYL GLYCOSIDE OF A DECAGALACTURONIC ACID, A MODEL COMPOUND FOR THE ENDOGENOUS PHYTOALEXIN ELICITOR-ACTIVE OLIGOGALACTURONIC ACIDS

Article abstract of DOI:10.1016/0008-6215(89)85010-4

Propyl O-(α-D-galactopyranosyluronic acid)-<(1->4)-O-(α-D-galactopyranosyluronic acid)>8-(1->4)-β-D-galactopyranosiduronic acid, a model compound for a phytoalexin-elicitor-active oligogalacturonic acid, was synthesized in a highly stereocontrolled manner