Conformational effects due to stereochemistry and C3-substituents in xylopyranoside derivatives as studied by NMR spectroscopy

Glycosaminoglycans contain a β- d -xylopyranose residue at its reducing end, which links the polysaccharide to the protein in proteoglycans. 2-Naphthyl β- d -xylopyranosides have shown inhibition of tumor growth and we herein investigate conformation and dynamics of compounds structurally and stereo...

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Veröffentlicht in:	Organic & biomolecular chemistry 2014-01, Vol.12 (4), p.831-835
Hauptverfasser:	Rönnols, Jerk, Manner, Sophie, Ellervik, Ulf, Widmalm, Göran
Format:	Artikel
Sprache:	eng
Schlagworte:	Carbohydrate Conformation Chemical Sciences Kemi Magnetic Resonance Spectroscopy Natural Sciences Naturvetenskap Stereoisomerism Thermodynamics Xylose - analogs & derivatives Xylose - chemistry
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