The title trisaccharide glycosides were needed for studies of the interactions of &tins, receptor sites for bacteriophages with Salmonella lipopolysaccharide corespecificity, and correlation of n.m.r. chemical shifts and structure. The methods used in the syntheses were conventional. Thus, 2,3,4,6-
Synthetic Antigens: Synthesis of 4-Aminophenyl O -α-D-Mannopyranosyl-(1→2)- O -α-D-mannopyranosyl-(1→6)- O -α-D-Mannopyranoside and A Related Di- and A Trisaccharide
✍ Scribed by Khan, Shaheer H.; Piskorz, Conrad F.; Matta, Khushi L.
- Book ID
- 127103743
- Publisher
- Taylor and Francis Group
- Year
- 1994
- Tongue
- English
- Weight
- 472 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0732-8303
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## Abstract NMR experiments such as steady state NOE experiments and spin lattice ^1^H relaxation time measurements were performed on the synthetic disaccharide 10 that constitutes part of the polysaccharide backbone in fungal mannans. The spectro‐scopic data were compared with a theoretical model