843674-44-2

Upstream product

• 201135-20-8 methyl 2,3,4-tri-O-benzyl-7,8-dideoxy-α-D-manno-oct-7-enopyranoside 
• 34212-64-1 methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 40653-15-4 methyl 2,3,4-tri-O-benzyl-α-D-manno-hexodialdo-1,5-pyranoside 
• 843674-42-0 1,6-anhydro-2,3,4-tri-O-benzyl-7,8-dideoxy-β-D-manno-oct-7-enopyranose 
• 843674-43-1 1,6-anhydro-2,3,4-tri-O-benzyl-L-glycero-β-D-manno-heptopyranose 
• 108-24-7 acetic anhydride 

Downstream Products

• 215381-22-9 (2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-(1->4)-7-O-acetyl-1,6-anhydro-2-O-benzyl-L-glycero-β-D-manno-heptopyranose 
• 215381-19-4 (2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-(1->4)-7-O-acetyl-1,6-anhydro-2,3-O-isopropylidene-L-glycero-β-D-manno-heptopyranose 
• 215381-20-7 (2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-(1->4)-7-O-acetyl-1,6-anhydro-L-glycero-β-D-manno-heptopyranose 

Relevant academic research and scientific papers

Synthesis of the branched trisaccharide L-glycero-α-D-manno- heptopyranosyl-(1 → 3)- [β-D-glucopyranosyl-(1 → 4)]-L-glycero-α-D-manno-heptopyranose, protected to allow flexible access to Neisseria and Haemophilus LPS inner core structures

An efficient synthesis of the protected branched trisaccharide (2′S,3′S)-(7-O-benzyl-6-O-chloroacetyl-3,4-O-(2′, 3′-dimethoxybutane-2′,3′-diyl)-2-O-p-methoxybenzyl-L-glycero- α-D-manno-heptopyranosyl)-(1 → 3)-[(2,3,4,6-tetra-O-benzoyl-β-D- glucopyranosyl)