346441-52-9

Upstream product

• 220903-22-0 6-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl trichloroacetimidate 
• 346441-51-8 1-O-allyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranose 
• 40246-29-5 methyl 2-O-benzoyl-3,4,6-tetra-O-benzyl-α-D-mannopyranoside 
• 346441-50-7 allyl 6-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranoside 
• 220903-20-8 1,6-di-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranose 
• 346441-46-1 6-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranose 

Downstream Products

• 346441-53-0 allyl O-(2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-(1→6)-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Facile synthesis of a comb-like mannohexaose: A trimer of the disaccharide repeating unit of the cell-wall mannans of Aphanoascus mephitatus and related species

An efficient method for the preparation of a comb-like mannohexaose having α-(1→6) and α-(1→2) linkages has been described using 6-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl trichloroacetimidate as the key glycosyl donor in an 'inverse Schmidt' procedure.