503456-90-4

Upstream product

• 100-39-0 benzyl bromide 
• 503456-85-7 C₃₂H₂₈N₂O₉S 
• 503456-87-9 methyl 2,3,6-tri-O-benzoyl-4-deoxy-4-C-allyl-α-D-mannopyranoside 
• 503456-88-0 methyl 4-C-allyl-2,3,6-tri-O-benzyl-4-deoxy-α-D-mannopyranoside 
• 503456-80-2 methyl 2,3,6-tri-O-benzyl-4-deoxy-4-C-[(E)-prop-1-en-1-yl]-α-D-mannopyranoside 
• 503456-79-9 methyl 2,3,6-tri-O-benzyl-4-deoxy-4-C-formyl-α-D-mannopyranoside 
• 3396-68-7 methyl 2,3,6-tri-O-benzoyl-α-D-mannopyranoside 
• 6160-65-2 1,1'-Thiocarbonyldiimidazole 
• 503456-89-1 methyl 2,3,6-tri-O-benzyl-4-deoxy-4-C-[(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)(hydroxy)methyl]-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of the C-linked disaccharide α-D-man-(1→4)-D-man employing a SmI2-mediated C-glycosylation step: En route to cyclic C-oligosaccharides

Investigations are reported on the assembly of the C-linked disaccharide α-D-Man-(1→4)-D-Man, representing the first steps in our projected synthesis of a cyclic C-oligomer containing repeating units of this C-dimer. The key step in this synthesis uses a