109526-95-6

Upstream product

• 100-39-0 benzyl bromide 
• 112612-45-0 methyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 100-44-7 benzyl chloride 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 86447-92-9 methyl 4-O-benzyl-6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 

Downstream Products

• 109443-32-5 D-erythro-2-benzyloxy-3-((S)-1-methoxy-2-oxo-ethoxy)-butyraldehyde 
• 144993-44-2 methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside 
• 21317-50-0 methyl 2,3,6-trideoxy-α-D-erythro-hexopyranoside 
• 73889-45-9 methyl 4-O-benzyl-2,3,6-trideoxy-α-D-erythro-hexopyranoside 
• 148431-61-2 methyl 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 151803-47-3 methyl 4-O-benzyl-6-deoxy-3-O-methyl-α-D-mannopyranoside 
• 151803-49-5 methyl 3,4-di-O-benzyl-6-deoxy-2-O-<(methylthio)thiocarbonyl>-α-D-mannopyranoside 
• 151803-48-4 methyl 4-O-benzyl-6-deoxy-3-O-methyl-2-O-<(methylthio)thiocarbonyl>-α-D-mannopyranoside 
• 151803-51-9 methyl 3,4-di-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 151803-50-8 methyl 4-O-benzyl-2,6-dideoxy-3-O-methyl-α-D-arabino-hexopyranoside 
• 152174-28-2 1,3-di-O-acetyl-2,4-di-O-benzyl-α-D-rhamnopyranose 

Relevant academic research and scientific papers

Synthesis of a Trisaccharide Repeating Unit of the O-Antigen from Burkholderia multivorans and Its Oligomers

Burkholderia multivorans is a Gram-negative bacterium, and an important opportunistic human pathogen that can cause fatal infections. Its O-antigens are useful templates for the development of carbohydrate-based vaccines. A highly convergent and efficient

Synthesis of O-α-D-Rhap-(1 → 3)-O-α-D-Rhap-(1 → 2)-O-α-D-Rhap-(1 → 12)-oxydodecanoyl-bovine serum albumin

The title compound (19), a conjugate of a trisaccharide based upon the repeating trisaccharide of α-D-rhamnose, which comprises the polysaccharide portion of 'A-band' lipopolysaccharide from a mutant (AK1401) of Pseudomonas aeruginosa, strain PAO1, with b

Synthesis of the Methyl α-D-Glycosides of Amicetose, Perosamine and Janose

New methods for the synthesis of tri- and di-deoxy sugar, namely methyl α-D-amicetoside, methyl α-D-perosaminoside and methyl α-D-janoside are described.The readily available methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside has been used as chiral