417711-22-9

Upstream product

• 117124-70-6 methyl 2,3-di-O-benzoyl-6-deoxy-6-fluoro-β-D-galactopyranoside 
• 417711-21-8 1,4-di-O-acetyl-2,3-di-O-benzoyl-6-deoxy-6-flouoro-α-D-galactopyranose 

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 
• 417711-25-2 benzyl 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-mannopyranoside 
• 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 

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