113776-63-9

Upstream product

• 113765-20-1 allyl 6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranoside 
• 113765-17-6 6-O-acetyl-2,3,4-tri-O-benzyl-α-D-galactopyranosyl fluoride 
• 122955-99-1 (2R,3R,4S,5S,6R)-2-Allyloxy-3,4,5-tris-benzyloxy-6-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-pyran 
• 122955-98-0 allyl 6-O-(4,4'-dimethoxytriphenylmethyl)-β-D-galactopyranoside 
• 113829-63-3 allyl 2,3,4-tri-O-benzyl-β-D-galactopyranoside 
• 113765-26-7 allyl 6-O-acetyl-2,3,4-tri-O-benzyl-β-D-galactopyranoside 
• 88567-49-1 6-O-acetyl-2,3,4-tri-O-benzyl-α/β-D-galactopyranoside 
• 97817-99-7 allyl 2,3-di-Ο-benzyl-β-D-galactopyranoside 
• 2595-07-5 allyl β-D-galactopyranoside 

Relevant academic research and scientific papers

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

Propyl O-(α-D-galactopyranosyluronic acid)-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

A HIGHLY EFFICIENT, PRACTICAL, AND STEREOSELECTIVE APPROACH TO THE SYNTHESIS OF α 1 --> 4 LINKED GALACTOOLIGOSACCHARIDES

Exclusive formation of α14 linked galactopyranosyl oligosaccharides could be achieved by employing glycosyl fluorides.The observed diastereofacial selectivity was explained in terms of the nucleophilic attack of glycosyl acceptors toward convex face of the glycosyl fluorides.