83075-57-4

Upstream product

• 100-39-0 benzyl bromide 
• 4153-24-6 1,2,3,4-tetra-O-methyl-α-D-glucopyranose 
• 6984-43-6 (2S,3R,4S,5R,6R)-2,3,4,5-tetramethoxy-6-((trityloxy)methyl)tetrahydro-2H-pyran 
• 1261355-42-3 phenyl 6-O-benzyl-2,3,4-tri-O-methyl-1-thio-β-D-glucopyranoside 
• 1393471-82-3 methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1->4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 74-88-4 methyl iodide 
• 1261355-91-2 methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1->4)-(methyl b-D-glucopyranosyluronate)-(1->4)-2,6-di-O-benzyl-3-deoxy-3-C-(methylsulfonatomethyl)-α-D-glucopyranoside 
• 1261355-89-8 methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1->4)-(methyl 2,3-di-O-acetyl-β-D-glucopyranosyluronate)-(1->4)-2,6-di-O-benzyl-3-deoxy-3-C-(methyl sulfonatomethyl)-α-D-glucopyranoside 

Downstream Products

• 541550-93-0 6-O-benzyl-2,3,4,5-tetra-O-methyl-D-gluconic acid 
• 541550-92-9 6-O-benzyl-2,3,4-tri-O-methyl-D-glucono-1,5-lactone 
• 74342-19-1 Methyl-6-C-<(S)-α-hydroxybenzyl>-2,3,4-tri-O-methyl-α-D-glucopyranosid 
• 74342-19-1 Methyl-6-C-<(R)-α-hydroxybenzyl>-2,3,4-tri-O-methyl-α-D-glucopyranosid 

Relevant academic research and scientific papers

Anti-coagulation pentasaccharide and preparing method and medical application thereof

The invention relates to a synthesized pentasaccharide compound, salt thereof, and application of the pentasaccharide compound in preparing medicines for preventing and/or treating blood coagulation disorder related diseases.

Synthesis of the non-reducing end trisaccharide of the antithrombin-binding domain of heparin and its bioisosteric sulfonic acid analogues

A glucoronic acid-containing trisaccharide related to the antithrombin-binding DEFGH domain of heparin and its methanesulfonic acid analogues were synthesized. Trisaccharides without sulfonic acid content or possessing a sulfonatomethyl moiety at position

Synthesis of 2,3,4,5-tetra-O-methyl-D-glucono-1,6-lactone as a monomer for the preparation of copolyesters

2,3,4,5-Tetra-O-methyl-D-glucono-1,6-lactone has been prepared as a crystalline compound in acceptable yield by two different routes. An initial assay of copolymerization with L-lactide by ring-opening polymerization was carried out. The incorporation of the carbohydrate monomer into the polymer chain was about 2%.