219808-90-9

Upstream product

• 89821-77-2 Allyl 4-O-benzyl-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 865-50-9 iodomethane-d3 
• 219808-89-6 4-O-benzyl-2,3-O-isopropylidene-α-L-rhamnopyranose 

Downstream Products

• 219808-96-5 (2H3)methyl (2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1-> 2)-3,4-di-O-benzyl-α-L-(2-2H)rhamnopyranoside 
• 219808-97-6 methyl (2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1-> 2)-3,4-di-O-benzyl-α-L-(2-2H)rhamnopyranoside 
• 219808-93-2 (2H3)methyl 3,4-di-O-benzyl-β-L-(2-2H)rhamnopyranoside 
• 219808-94-3 (2H3)methyl 3,4-di-O-benzyl-α-L-(2-2H)rhamnopyranoside 
• 219808-92-1 (2H3)methyl 3,4-di-O-benzyl-β-L-rhamnopyranoside 
• 219808-95-4 methyl 3,4-di-O-benzyl-α-L-(2-2H)rhamnopyranoside 
• 219808-91-0 (2H3)methyl 4-O-benzyl-β-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of site-specific, deuterium-substituted α-l-Rhap-(12)-α-L-Rhap-OMe

The disaccharide α-l-Rhap-(12)-α-l-(2-2H)Rhap-OMe has been synthesized. The site-specific deuteration was performed at C-2 by reduction of a suitably protected β-linked 2-ulose derivative. In addition, α-l-Rhap-(12)-α-l-(2-2H)Rhap-O(2H3)Me was also synthesized. Copyright (C) 1998 Elsevier Science Ltd.