69359-17-7

Upstream product

• 69401-46-3 benzyl 2,4-di-O-benzyl-α-D-mannopyranoside 
• 65827-59-0 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride 
• 69359-16-6 C₈₅H₉₀O₁₈ 

Downstream Products

• 141990-25-2 C₁₃₉H₁₄₆O₂₈ 
• 76542-64-8 C₁₄₅H₁₅₆N₂O₅₀ 

Relevant academic research and scientific papers

Synthesis of a nonasaccharide with two Lewis x trisaccharides anchored onto a branched trimannoside

Double condensation of phenyl 3,4,6-tri-O-benzyl-2-O-[6-O-benzyl-2-deoxy-2-phthalimido-4-O-(2,3,4,6- tetra-O-benzoyl-β-D-galactopyranosyl)-3-O-(2,3,4-tri-O-benzyl-α-L-fu copyranosyl)-β-D-glucopyranosyl]-1-thio-α-D-mannopyranoside 31 with methyl 2,4-di-O-b

Synthesis of an octasaccharide fragment of high-mannose-type glycans of glycoproteins

O-(α-D-Mannopyranosyl)-(1->2)-O-(α-D-mannopyranosyl)-(1->3)-O-2)-O-(α-D-mannopyranosyl)-(1->6)>-O-(α-D-mannopyranosyl)-(1->6)-O-(β-D-mannopyranosyl)-(1->4)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->4)-2-acetamido-2-deoxy-glu

Synthesis of a tri- and a hepta-saccharide which contain alpha-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteins.

Reaction of a thioglycoside with methyl trifluoromethanesulfonate (methyl triflate) in the presence of a hydroxyl compound is an efficient glycosylation method. Thus, methyl triflate-promoted condensation of ethyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-1