934587-99-2

Upstream product

• 28541-75-5 p-methoxyphenyl α-D-mannopyranoside 
• 530-26-7 D-Mannose 
• 150-76-5 4-methoxy-phenol 
• 934587-86-7 2-iodomethyl-6-(4-methoxy-phenoxy)-tetrahydro-pyran-3,4,5-triol 
• 934587-87-8 4-methoxyphenyl 1-α-D-rhamnopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 934588-00-8 C₃₄H₃₂O₈ 
• 934588-03-1 C₂₇H₂₆O₈ 
• 1304123-37-2 4-methoxyphenyl 2,4-di-O-acetyl-3-O-benzyl-α-D-rhamnopyranoside 
• 1304123-43-0 4-methoxyphenyl 2,3,4-tri-O-acetyl-6-deoxy-α-D-altopyranoside 
• 1304123-41-8 4-methoxyphenyl 2,4-di-O-acetyl-3-O-trifluoromethanesulfonyl-α-D-rhamnopyranoside 
• 1304123-39-4 4-methoxyphenyl 2,4-di-O-acetyl-α-D-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of 6-deoxy-d-altrose used as an authentic sample to identify an unknown monosaccharide isolated from the fruiting body of an edible mushroom

Here, we describe the synthesis of 6-deoxy-D-altrose and its subsequent use as an authentic sample to verify the structure of a monosaccharide newly isolated from the fruiting body of an edible mushroom. D-Rhamnopyranoside, converted from D-mannopyranosid

Practical synthesis of valuable d-rhamnoside building blocks for oligosaccharide synthesis

The efficient synthesis of d-rhamnoside and the corresponding methods for its regioselective protections and deprotections have been developed in order to provide key building blocks for complex oligosaccharide syntheses toward vaccines against bacterial infections.