158610-40-3

Upstream product

• 89821-78-3 allyl 4-O-benzyl-α-L-rhamnopyranoside 
• 106-95-6 allyl bromide 

Downstream Products

• 158610-41-4 allyl 3-O-allyl-4-O-benzyl-2-O-methyl-α-L-rhamnopyranoside 
• 158610-45-8 Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[(2S,3S,4R,5R,6S)-3-benzyloxy-6-((2S,3S,4R,5R,6R)-3-benzyloxy-5,6-dimethoxy-2-methyl-tetrahydro-pyran-4-yloxy)-5-methoxy-2-methyl-tetrahydro-pyran-4-yloxy]-tetrahydro-pyran-3-yl ester 
• 158610-46-9 methyl 4-O-benzyl-2-O-methyl-3-O-<4-O-benzyl-2-O-methyl-3-O-(β-D-glucopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 
• 158610-43-6 methyl 4-O-benzyl-2-O-methyl-3-O-(3-O-acetyl-4-O-benzyl-2-O-methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 
• 158610-44-7 methyl 4-O-benzyl-2-O-methyl-3-O-(4-O-benzyl-2-O-methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

SYNTHESIS OF TERMINAL OLIGOSACCHARIDES FROM TYPE SPECIFIC LIPOOLIGOSACCHARIDE OF MYCOBACTERIUM TUBERCULOSIS

The coupling reaction between 1,3-di-O-acetyl-4-O-benzyl-2-O-methyl-α-L-rhamnopyranose (9) and methyl 4-O-benzyl-2-O-methyl-α-L-rhamnopyranoside (4) was carried out in the presence of boron trifluoride-etherate followed by deacetylation to give the disacc