80738-49-4

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 86172-79-4 (2S,3S,4S,5R,6R)-2-Methoxy-4-trityloxy-6-trityloxymethyl-tetrahydro-pyran-3,5-diol 
• 100-44-7 benzyl chloride 
• 73395-14-9 methyl (R,R)-2,3:4,6-di-O-benzylidene-α-D-mannopyranoside 
• 15038-71-8 methyl 2-O-benzyl-(R)-4,6-O-benzylidene-α-D-mannopyranoside 
• 73395-15-0 methyl endo(phenyl)-2,3:4,6-di-O-benzylidene-α-D-mannopyranoside 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 58341-67-6 methyl 2,4-di-O-benzyl-α-D-mannopyranoside 
• 108-24-7 acetic anhydride 
• 227306-95-8 methyl 2,4-di-O-benzyl-3,6-di-O-trityl-α-D-mannopyranoside 

Downstream Products

• 79218-66-9 3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-mannopyranosyl chloride 
• 79218-64-7 C₆₉H₇₈O₂₀ 
• 80738-57-4 methyl 3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-6-O-(3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside 
• 80738-58-5 methyl 6-O-(2,4-di-O-benzyl-α-D-mannopyranosyl)-3-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside 
• 80738-53-0 methyl 3,6-di-O-(2,4-di-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside 
• 80738-51-8 Acetic acid (2R,3R,4S,5S,6S)-2-acetoxymethyl-3,5-bis-benzyloxy-6-((2R,3S,4S,5S,6S)-3,5-bis-benzyloxy-4-hydroxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-4-yl ester 
• 80738-52-9 methyl 2,4-di-O-benzyl-6-O-(2,4-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside 
• 78962-39-7 methyl α-D-mannopyranosyl-(1→6)-α-D-mannopyranoside 
• 68601-74-1 methyl 3,6-di-O-(α-D-mannopyranosyl)-α-D-mannopyranoside 
• 869207-86-3 p-(methoxycarbonyl)phenyl 2,4-di-O-benzyl-α-D-mannopyranoside 
• 80779-87-9 1,3,4,6-tetra-O-acetyl-2-O-benzyl-α-D-mannopyranoside 
• 80738-50-7 1,3,6-tri-O-acetyl-2,4-di-O-benzyl-α-D-mannopyranose 

Relevant academic research and scientific papers

Efficient synthesis of man2, man3, and man 5 oligosaccharides, using mannosyl iodide donors

A highly efficient protocol for making Man3 and Man5 oligosaccharides with use of orthogonally protected glycosyl iodide donors has been developed. Glycosylation of a C-2-O-acetyl mannosyl iodide donor in the presence of silver trifl

Ditritylation of Methyl and Benzyl α-D-Gluco-, -Manno-, and -Galactopyranosides and Preparation of Their Partially Benzylated Derivatives

The ditritylation of methyl and benzyl α-D-gluco-, -manno-, and -galactopyranosides with trityl chloride in pyridine at 70 deg C proceeds in a regioselective manner to give the 2,6-ditrityl ethers of the glucosides, the 3,6-ones of the mannosides, and bot

RECONSTRUCTION OF GLYCAN CHAINS OF GLYCOPROTEIN BRANCHING MANNOPENTAOSIDE AND MANNOHEXAOSIDE

Synthetic routes to the branching mannopentaoside 4 and mannohexaoside 5 are described employing properly protected mannobioside 13 as a key intermediate.