109923-93-5

Upstream product

• 6294-16-2 D-galacturonic acid 
• 100-51-6 benzyl alcohol 
• 489-91-8 D-galacturonic acid 

Downstream Products

• 141118-09-4 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl (benzyl 2,3,4-tri-O-benzyl-α-D-galactopyranosid)uronate 
• 141118-08-3 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl (benzyl 2,3,4-tri-O-benzyl-α-D-galactopyranosid)uronate 
• 141118-12-9 2,3,4,6-tetra-O-benzyl-β-D-mannopyranosyl (benzyl 2,3,4-tri-O-benzyl-α-D-galactopyranosid)uronate 
• 141118-11-8 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl (benzyl 2,3,4-tri-O-benzyl-α-D-galactopyranosid)uronate 
• 141118-10-7 benzyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-α-D-galactopyranoside 
• 53929-41-2 benzyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-α-D-galactopyranoside 
• 141118-13-0 benzyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-β-D-mannopyranosyl)-α-D-galactopyranoside 
• 53929-42-3 benzyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-galactopyranoside 
• 141118-06-1 3-nitropyridyl-2-(benzyl 2,3,4-tri-O-benzyl-α-D-galactopyranosid)thiouronate 
• 141118-07-2 4-nitrophenyl (benzyl 2,3,4-tri-O-benzyl-α-D-galactopyranosid)uronate 
• 141118-05-0 benzyl 2,3,4-tri-O-benzyl-α-D-galactopyranosiduronic acid 
• 109959-33-3 sodium (phenylmethyl α-D-galactopyranosid)uronate 

Relevant academic research and scientific papers

Redox Glycosidation: Stereoselective Syntheses of 1 -> 6 Linked Disaccharides via Thionoester Intermediates

Perbenzyl derivatives of the disaccharides benzyl 6-O-(α(and β)-D-glucopyranosyl)-α-D-galactopyranoside and benzyl 6-O-(α(and β)-D-mannopyranosyl)-α-D-galactopyranoside were each prepared in a stereoselective manner by acylation, thionation, and reductive

NMR Studies of the Interaction of Metal Ions with Poly(1,4-hexuronates). VI. Lanthanide(III) Complexes of Sodium (Methyl α-D-galactopyranosid)uronate and Sodium (Phenylmethyl α-D-galactopyranosid)uronate

Our previous suggestion that lanthanide(III) ions form 1:3 complexes of axial symmetry with sodium (methyl α-D-galactopyranosid)uronate has been supported by further NMR studies and model building.LIS experiments also showed that the phenylmethyl glycoside forms similar complexes.Dysprosium(III)-induced 17O NMR shifts indicated that the lanthanide complexes contain three coordinated water molecules.By cooling a methanolic solution of the methyl glycoside containing Eu(3+) ions, a precipitate was formed which, it was possible to show, had 1:3 stoichiometry.