125519-98-4Relevant articles and documents
Synthesis of a Trisaccharide Repeating Unit of the O-Antigen from Burkholderia multivorans and Its Oligomers
Zhang, Xin,Gu, Guofeng,Guo, Zhongwu
, p. 7075 - 7085 (2015/11/16)
Burkholderia multivorans is a Gram-negative bacterium, and an important opportunistic human pathogen that can cause fatal infections. Its O-antigens are useful templates for the development of carbohydrate-based vaccines. A highly convergent and efficient
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-
Investigation of Different Synthetic Approaches towards Methyl 2,6-Dideoxy-α-D-arabino- and -α-D-lyxo-hexopyranosides
Kjoelberg, Ove,Neumann, Klaus
, p. 721 - 727 (2007/10/02)
New synthetic routes for making available different methyl 2,6-dideoxyhexopyranosides are reported.Starting with methyl 6-deoxy-2,3-O-isopropylidene-α-D-manno- and -α-D-talo-pyranoside the respective methyl 2,6-dideoxy-α-D-arabino- and α-D-lyxo-hexopyrano