138098-80-3

Upstream product

• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 73983-19-4 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose 
• 72599-87-2 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl chloride 
• 71715-58-7 3,4-di-O-benzyl-6-deoxy-1,2-O-<(R,S)-ethylidene>-β-L-mannopyranose 
• 79080-88-9 3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose 
• 71715-60-1 1,2-O-ethylidene-β-L-rhamnopyranose 
• 100-44-7 benzyl chloride 

Downstream Products

• 148431-63-4 O-(3,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl)-(1->6)-1,2;3,4-di-O-isopropylidene-α-D-galactopyranose 
• 125519-98-4 methyl 3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis, conformational analysis, and the glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-β-L- and β-D-rhamnopyranoses

1,2-Anhydro-3,4-di-O-benzyl-α-L-rhamnopyranose was synthesized from L-rhamnose, while the D-enantiomer was synthesized from methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside. For both of the syntheses, the key intermediates were 2-O-acetyl-3,4-di-O-