417711-25-2

Upstream product

• 417711-24-1 benzyl 4-O-acetyl-2,3-di-O-benzoyl-6-deoxy-6-fluoro-β-D-galactopyranosyl-(1->4)-6-O-benzoyl-2,3-O-isopropylidene-α-D-mannopyranoside 
• 417711-21-8 1,4-di-O-acetyl-2,3-di-O-benzoyl-6-deoxy-6-flouoro-α-D-galactopyranose 
• 417711-22-9 C₂₂H₂₀BrFO₇ 
• 417711-23-0 benzyl 6-O-benzoyl-2,3-O-isopropylidene-α-D-mannopyranoside 
• 117124-70-6 methyl 2,3-di-O-benzoyl-6-deoxy-6-fluoro-β-D-galactopyranoside 
• 139722-11-5 benzyl 2,3,4,6-bis(di-O-isopropylidene)-α-D-mannopyranoside 
• 139722-12-6 benzyl 2,3-O-isopropylidene-α-D-mannopyranoside 
• 15548-45-5 (2S,3S,4S,5S,6R)-2-benzyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 

Downstream Products

• 417711-26-3 4-O-acetyl-2,3-di-O-benzoyl-6-deoxy-6-fluoro-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose 

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