121360-05-2

Upstream product

• 475672-25-4 allyl L-rhamnopyranoside 
• 114284-06-9 allyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 98-88-4 benzoyl chloride 
• 100639-25-6 allyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 114284-07-0 allyl 4-O-benzoyl-α-L-rhamnopyranoside 
• 74-88-4 methyl iodide 

Downstream Products

• 121360-07-4 allyl O-(4-O-acetyl-2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-4-O-benzoyl-3-O-methyl-α-L-rhamnopyranoside 
• 536992-33-3 C₂₄H₂₆O₇ 
• 121360-09-6 allyl O-(2,4-di-O-acetyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1-4)-O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-4-O-benzoyl-3-O-methyl-α-L-rhamnopyranoside 
• 121360-08-5 allyl O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-4-O-benzoyl-3-O-methyl-α-L-rhamnopyranoside 
• 121333-93-5 allyl O-(3,6-di-O-methyl-β-D-glucopyranosyl)-(1-4)-O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-3-O-methyl-α-L-rhamnopyranoside 
• 536992-41-3 C₆₆H₈₄O₁₆ 
• 536992-38-8 C₆₆H₈₄O₁₅ 
• 536992-35-5 C₂₃H₂₂Cl₃NO₇ 

Relevant academic research and scientific papers

Synthesis of monomethylated dioscin derivatives and their antitumor activities

All possible eight monomethylated dioscin derivatives (1-8) were synthesized. Their inhibitory activities against P388 and A-549 cells were determined, and the results indicate that six of the eight hydroxyls of dioscin are the 'key polar groupings' for tumor inhibitory activities.

Chemical synthesis of an artificial antigen containing the trisaccharide hapten of Mycobacterium leprae.

The trisaccharide allyl O-(3,4-di-O-methyl-beta-D-glucopyranosyl)-(1----4)-O-(2,3-di-O-methyl-al pha-L- rhamnopyranosyl)-(1----2)-3-O-methyl-alpha-L-rhamnopyranoside was synthesized from partially methylated monosaccharide derivatives. Condensation of 1,4