80859-31-0

Upstream product

• 87190-67-8 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-O-trichloroacetimidate 
• 80859-30-9 benzyl 3,4-di-O-benzyl-α-D-mannopyranoside 
• 65529-49-9 benzyl 2,3(R):4,6(R)-di-O-benzylidene-α-D-mannopyranoside 
• 130539-42-3 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl fluoride 
• 10028-45-2 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl bromide 

Downstream Products

• 80859-32-1 benzyl 2,6-di-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-3,4-di-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of multiantennary complex type N-Glycans by use of modular building blocks

A modular set of oligosaccharide building blocks was developed for the synthesis of multiantennary Nglycans of the complex type, which are commonly found on glycoproteins. The donor building blocks were laid out for the elongation of a core trisaccharide

Synthesis of three oligosaccharides that form part of the complex type of carbohydrate moiety of glycoproteins.

Silver trifluoromethanesulfonate-promoted condensation of 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranosyl bromide with benzyl 3,6-di-O-benzyl-alpha-D-mannopyranoside and benzyl 3,4-di-O-benzyl-alpha-D-mannopyranoside gave the protected 2,4-