72599-87-2Relevant articles and documents
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
Chen,Kong,Cao
, p. 107 - 117 (2007/10/02)
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-
Artificial Carbohydrate Antigens: Synthesis of Rhamnose Trisaccharide and Disaccharide Haptens common to Shigella flexneri O-Antigens
Josephson, Staffan,Bundle, David R.
, p. 297 - 301 (2007/10/02)
The rhamnose di- and tri-saccharide glycosides, α-L-Rham(p)-(1 --> 3)-α-L-Rham(p) and α-L-Rham(p)-(1 --> 2)-α-L-Rham(p)-(1 --> 3)-α-L-Rham(p), representing portions of the Shigella flexneri serogroup Y lipopolysaccharide repeating unit, have been synthesi