Stereoselective total synthesis of dodecagalacturonic acid, a phytoalexin elicitor of soybean

DOI: 10.1016/0008-6215(90)80135-P

Source and publish data:

Carbohydrate Research p. 147 - 159 (1990)

Update date:2022-08-04

Topics: phytoalexin Total synthesis Stereoselective

Authors:

Nakahara, Yoshiaki

Ogawa, Tomoya

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Article abstract of DOI:10.1016/0008-6215(90)80135-P

O-(α-D-Galactopyranosyluronic acid)-<(1-->4)-O-(α-D-galactopyranosyluronic acid)>₁₀-D-galactopyranuronic acid (1), an endogenous elicitor of the phytoalexin of soybean, was synthesized by way of highly stereoselective glycosylations that involv

Full text of DOI:10.1016/0008-6215(90)80135-P

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Product name:tert-butyldiphenylsilyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-galactopyranosyl)-<(1->4)-O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)>₂-(1->4)-6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranoside

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