82703-50-2

Upstream product

• 82703-49-9 benzyl 2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 13242-53-0 acetobromomannose 
• 61134-29-0 benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 82703-48-8 3,4,6-tri-O-benzyl-1,2-O-(1-benzyloxyethylidene)-β-D-mannopyranose 
• 61134-30-3 benzyl 3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 88293-80-5 3,4,6-tri-O-acetyl-1,2-O-(1-benzyloxyethylidene)-β-D-mannopyranose 
• 65827-59-0 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride 

Downstream Products

• 89068-14-4 C₁₁₁H₁₃₀O₄₄ 
• 82703-54-6 benzyl 2-O-(2-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 15548-39-7 α-D-mannopyranosyl-(1->2)-D-mannopyranoside 
• 82703-59-1 C₈₇H₉₈O₂₈ 

Relevant academic research and scientific papers

Multivalent glyconanoparticles with enhanced affinity to the anti-viral lectin Cyanovirin-N

Low-mannose (LM) structures were coupled to gold nanoparticles (Au NPs) to amplify the affinity of LMs with Cyanovirin-N (CV-N) lectins and to study the structures of CV-N variants CVNQ50C and CVNMutDB. The Royal Society of Chemistry

Sonication-assisted oligomannoside synthesis

We have investigated the use of sonication for the synthesis of oligomannosides. A convenient sonication- mediated glycosylation protocol that is applicable to traditional glycosylation methods has been developed. This protocol can be applicable for activ

SYNTHESIS OF LINEAR D-MANNOTETRAOSE AND D-MANNOHEXAOSE, PARTIAL STRUCTURES OF THE CELL-SURFACE D-MANNAN OF Candida albicans AND Candida utilis

Syntheses of linear D-manno-oligosaccharides, O-α-Man-(1-2)-O-α-Man-(1-2)-O-α-Man-(1-2)-Man and O-α-Man-(1-2)-O-α-Man-(1-2)-O-α-Man-(1-2)-O-α-Man-(1-2)-Man, which correspond to part of the structure of the cell-wall D-mannan chain of Candida utilis and Ca