83259-13-6

Upstream product

• 86861-45-2 1,6-Di-O-acetyl-3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranose 
• 86861-44-1 3-O-Allyl-1,6-anhydro-2,4-di-O-benzyl-β-D-mannopyranose 
• 86861-42-9 1,6-anhydro-2,4-di-O-benzyl-β-D-mannopyranose 
• 86900-44-9 1,6-anhydro-4-O-benzyl-β-D-mannopyranose 
• 58341-56-3 methyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 106444-74-0 methyl 2,4-di-O-benzyl-3-O-allyl-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 82228-10-2 methyl 3-O-allyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 106444-75-1 methyl 6-O-acetyl-3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranoside 

Downstream Products

• 83273-00-1 O-(2-O-Acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-> 6)-O-(3-O-allyl-2,4-di-O-benzyl-β-D-mannopyranosyl)-(1-> 4)-1,6-anhydro-2-azido-3-O-benzyl-2-desoxy-β-D-glucopyranose 
• 83259-21-6 O-(2-O-Acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-> 3)-O-(6-O-acetyl-2,4-di-O-benzyl-β-D-mannopyranosyl)-(1-> 4)-1,6-anhydro-2-azido-3-O-benzyl-2-desoxy-β-D-glucopyranose 
• 83259-20-5 4-O-(6-O-Acetyl-2,4-di-O-benzyl-β-D-mannopyranosyl-1,6-anhydro-2-azido-3-O-benzyl-2-desoxy-β-D-glucopyranose 
• 83259-18-1 4-O-(3-O-Allyl-2,4-di-O-benzyl-β-D-mannopyranosyl)-1,6-anhydro-2-azido-3-O-benzyl-2-desoxy-β-D-glucopyranose 
• 83259-15-8 1,6-Anhydro-2-azido-3-O-benzyl-4-O-(2,4-di-O-benzyl-β-D-mannopyranosyl)-2-desoxy-β-D-glucopyranose 
• 86861-55-4 O-(2-O-Acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-> 6)-O-(2,4-di-O-benzyl-β-D-mannopyranosyl)-(1-> 4)-1,6-anhydro-2-azido-3-O-benzyl-2-desoxy-β-D-glucopyranose 
• 83259-14-7 4-O-(6-O-Acetyl-3-O-allyl-2,4-di-O-benzyl-β-D-mannopyranosyl)-1,6-anhydro-2-azido-3-O-benzyl-2-desoxy-β-D-glucopyranose 
• 106444-76-2 8-methoxycarbonyloctyl-6-O-acetyl-3-O-allyl-2,4-di-O-benzyl-β-D-mannopyranosyl bromide 
• 106444-77-3 8-methoxycarbonyloctyl-6-O-acetyl-3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranosyl bromide 

Relevant academic research and scientific papers

Building Units of Oligosaccharides, CIX. - Synthesis of Modified Oligosaccharides of N-Glycoproteins for Substrate Specificity Studies of N-Acetylglucosaminyltransferase I

A series of modified derivatives of the trisaccharide octyl α-D-Man(1-->3)-6)>-β-D-Man were synthesized for substrate specificity studies of N-acetylglucosaminyltransferase I (GlcNAc-T I).The hydroxyl groups at C-3, C-4 and C-6 of the α(1-->3

Substrates for the differentiation of the N-acetylglucosaminyltransferases. Synthesis of βDGlcNAc(->2)αDMan(1->6)βDMan and βDGlcNAc(1->2)αDMan(1->6)3)βDMan glycosides

The trisaccharide βDGlcNAc(1->2)αDMan(1->6)βDMan (2) and the tetrasaccharide βDGlcNAc(1->2)αDMan(1->6)αDMan(1->3)>βDMan (3) have been chemically synthesized as their 8-methoxycarbonyloctyl glycosides.Compounds 2 and 3, both partial structures of naturally

Building Units of Oligosaccharides, XLVII. - Synthesis of Tri- and Tetrasaccharide Sequences of N-Glycoproteins Including a β-D-Mannosidic Linkage

The trisaccharides α-D-Man-p-(1 -> 6)-β-D-Man-p-(1 -> 4)-D-GlcNAc (37) and α-D-Man-p-(1 -> 3)-β-D-Man-p-(1 -> 4)-D-GlcNAc (43) as well as the key tetrasaccharide α-D-Man-p-(1 -> 3)- 6)>-β-D-Man-p-(1 -> 4)-D-GlcNAc (51), which are parts of th