220903-22-0

Upstream product

• 220903-20-8 1,6-di-O-acetyl-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 
• 545-06-2 trichloroacetonitrile 
• 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 
• 849208-13-5 octyl 3,4-di-O-benzyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 849208-15-7 octyl 3,4-di-O-benzyl-6-deoxy-2-O-methyl-6-phthalimido-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 849208-14-6 octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 849208-12-4 octyl 3,4-di-O-benzyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 849208-18-0 octyl 3,4-di-O-benzyl-6-deoxy-6-fluoro-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 849208-16-8 octyl 3,6-anhydro-4-O-benzyl-2-O-methyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 849208-11-3 octyl 6-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 346441-52-9 allyl 6-O-acetyl-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.

Facile syntheses of a hexasaccharide and a nonasaccharide related to the cell wall D-mannan of yeast Candida albicans

A highly efficient strategy for the preparation of D-manno-hexa- and nonasaccharides related to the cell wall D-mannan of yeast Candida albicans having α-(1→6)- and α-(1→2)-linkages has been developed using 6-O- acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl trichloroacetimidate (7) as the key glycosyl donor in the 'Inverse Schmidt' procedure.