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

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

Source and publish data:

Carbohydrate Research p. 95 - 114 (1989)

Update date:2022-08-05

Topics:

Authors:

Nakahara, Yoshiaki

Ogawa, Tomoya

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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

Full text of DOI:10.1016/0008-6215(89)85010-4

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