150730-92-0

Upstream product

• 69558-13-0 methyl 4-O-benzyl-3-O-methyl-α-L-rhamnopyranoside 
• 25019-69-6 methyl 4-O-benzyl-α-L-rhamnopyranoside 
• 545-06-2 trichloroacetonitrile 

Downstream Products

• 150966-53-3 Methyl 2,3-di-O-methyl-4-O-<4-O-benzyl-3-O-methyl-2-O-(2-O-acetyl-4-O-benzyl-3-O-methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 
• 150966-51-1 Methyl 2,3-di-O-methyl-4-O-(2-O-acetyl-4-O-benzyl-3-O-methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 
• 150966-54-4 Methyl 2,3-di-O-methyl-4-O-<4-O-benzyl-3-O-methyl-2-O-(4-O-benzyl-3-O-methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 
• 150966-55-5 Methyl 2,3-di-O-methyl-4-O-<4-O-benzyl-3-O-methyl-2-O-(4-O-benzyl-2,3-di-O-methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of the Oligosaccharide Segment of a Novel Phenolic Glycolipid Antigen from Mycobacterium haemophilum

The synthesis of the trisaccharide segment from Mycobacterium haemophilum phenolic glucolipid has been described.The synthesis of the disaccharide derivative 12 containing a free hydroxy group at C-2' was first examined by using 2-O-acetyl-4-O-benzyl-3-O-