172334-45-1Relevant articles and documents
Lipo-oligosaccharide of the Campylobacter lari type strain ATCC 35221. Structure of the liberated oligosaccharide and an associated extracellular polysaccharide
Aspinall, Gerald O.,Monteiro, Mario A.,Pang, Henrianna
, p. 245 - 264 (1995)
Lipo-oligosaccharide (LOS) from phenol-water extraction of cells of the Campylobacter lari type strain (ATCC 35221) was separated as a water-insoluble gel of low relative molecular mass (Mr) from a water-soluble extracellular polysaccharide of high Mr.Structural investigations were performed on the liberated oligosaccharide and the extracellular polysaccharide, variously using 1H, 13C, 31 P NMR spectroscopy, linkage analysis, and fast atom bombardment-mass spectrometry of permethylated derivatives of the glycans and their products of chemical and enzymic degradation.The following structures are proposed for the highly branched region of the LOS: and for the tetraglycosyl phosphate repeating unit of the extracellular polysaccharide: - -> 3)-β-D-Glc pNAc-(1 -> 2)-6-d-α-L-gul-Hep p-(1 -> 2)-3-d-β-D-threo-Pen p-(1 -> 3)-6-d-α-L-gul-Hep p->n - Keywords: Campylobacter lari type strain (ATCC 35221); Lipo-oligosaccharide; Extracellular polysaccharide; Tetraglycosyl phosphate polymer
Enantiospecific synthesis of both enantiomers of 2-benzyloxydihydropyran-3- ones from arabinose
Uhrig, Maria Laura,Varela, Oscar
, p. 893 - 898 (2007/10/03)
Approaches to the enantioselective synthesis of the useful building blocks (2R)- and (2S)-2-benzyloxy-2(H)-pyran-3(6H)-one (12 and 17, respectively) are described. The most direct and highly yielding route for the synthesis of 12 was based on the 'one-pot