521970-83-2

Upstream product

• 197895-54-8 methyl (2S,3S,4S,5R,6S)-3,4,5-tris(acetoxy)-6-[(trichloroethanimidoyl)oxy]oxane-2-carboxylate 
• 325704-78-7 pent-4-enyl 2-azido 2-deoxy-4,6-O-bennzylidene β-D-glucopyranoside 
• 21085-72-3 1-bromo-2,3,4-tri-O-acetyl-α-D-glucuronic acid methyl ester 
• 145840-43-3 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-glucopyranosyl trichloroacetimidate 
• 171032-74-9 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-D-glucopyranose 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 72692-06-9 methyl 2,3,4-tri-O-acetyl-D-glucopyranuronate 

Downstream Products

• 521970-84-3 pent-4-enyl 4,6-O-benzylidene 2-deoxy-2-N-acetyl 3-O-(methyl 2,3,4-tri-O-acetyl β-D-glucopyranosyluronate)-β-D-glucopyranoside 

Relevant academic research and scientific papers

Hyaluronan-based glycoclusters as probes for chemical glycobiology

A strategy is described for the synthesis of β-(1,3)-GlcA-GlcNAc dimeric and tetrameric glycoclusters through the conjugation of disaccharide groups onto a diaminodiamide aromatic scaffold by reductive amination.

Homodimerization of hyaluronan and heparan sulfate derivatives by olefin metathesis reaction

Hyaluronan and heparan sulfate disaccharides of the type β-D-glucuronic acid-(1→3)-N-acetyl-β-D-glucosamine and α-L-iduronic acid-(1→4)-N-acetyl-β-D-glucosamine, respectively, with an n-pentenyl group at the reducing end have been synthesized. Homodimeriz