743432-03-3

Upstream product

• 743432-00-0 allyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1-> 6)-3-O-benzoyl-2-O-chloroacetyl-α-D-mannopyranoside 
• 743431-96-1 allyl 3-O-benzoyl-4,6-di-O-benzylidene-α-D-mannopyranoside 
• 743431-98-3 allyl-3-O-benzoyl-2-O-chloroacetyl-α-D-mannopyranoside 
• 81600-93-3 allyl 4,6-di-O-benzylidene-α-D-mannopyranoside 
• 98-88-4 benzoyl chloride 
• 743432-01-1 allyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-O-chloroacetyl-α-D-mannopyranoside 

Downstream Products

• 743432-12-4 allyl 2-O-acetyl-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl-(1->-6)-3,4-di-O-benzoyl-2-O-chloroacetyl-α-D-mannopyranosyl-(1-> 6)-2-O-acetyl-3-O-benzoyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Facile synthesis of arabinomannose penta- and decasaccharide fragments of the lipoarabinomannan of the equine pathogen, Rhodococcus equi

Pentasaccharide repeating unit 20 of the lipoarabinomannan from the equine pathogen, Rhodococcus equi, and its dimer 31, were synthesized. The pentasaccharide was obtained by assembling a benzoylated 2,6-branched mannosyl trisaccharide acceptor 13 with a