417710-84-0

Upstream product

• 417710-82-8 methyl 2,6-di-O-benzoyl-3-deoxy-α-D-arabino-hexopyranoside 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 72904-78-0 methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside 
• 144370-68-3 methyl-[O²-benzoyl-O⁴,O⁶-((R)-benzylidene)-α-D-arabino-3-deoxy-hexopyranoside] 
• 98-88-4 benzoyl chloride 
• 98757-54-1 methyl 2-O-benzoyl-3-deoxy-α-D-arabino-hexopyranoside 

Downstream Products

• 417710-85-1 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-1-O-acetyl-2,6-di-O-benzoyl-3-deoxy-α-D-arabino-hexopyranose 

Relevant academic research and scientific papers

Parasite glycoconjugates. Part 12. Synthesis of deoxy, fluorodeoxy and aminodeoxy disaccharide phosphates, substrate analogues for the elongating α-D-mannopyranosylphosphate transferase in the Leishmania

A set of phosphodisaccharides, structural analogues of the β-D-galactosyl-(1→4)-α-D-mannosyl phosphate 1, are synthesized using the Koenigs-Knorr method for the glycosylation reactions and the glycosyl hydrogenphosphonate method for phosphorylation. The c