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Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study

The title compound, C(13)H(24)O(10) is the methyl glycoside of a structural element α-l-Fucp-(1→ 3)-α-d-Galp making up two thirds of the repeating unit in the capsular polysaccharide of Klebsiella K63. The conformation of the title compound is described by the glycosidic torsion angles ϕ(H) = 55 (1)...

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Autores principales: Eriksson, Lars, Widmalm, Göran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275268/
https://www.ncbi.nlm.nih.gov/pubmed/22347124
http://dx.doi.org/10.1107/S1600536812002279
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author Eriksson, Lars
Widmalm, Göran
author_facet Eriksson, Lars
Widmalm, Göran
author_sort Eriksson, Lars
collection PubMed
description The title compound, C(13)H(24)O(10) is the methyl glycoside of a structural element α-l-Fucp-(1→ 3)-α-d-Galp making up two thirds of the repeating unit in the capsular polysaccharide of Klebsiella K63. The conformation of the title compound is described by the glycosidic torsion angles ϕ(H) = 55 (1)° and ψ(H) = −24 (1)°. The hy­droxy­methyl group in the galactose residue is present in the gauche–trans conformation. In the crystal, O—H⋯O hydrogen bonds connect the disaccharide units into chains along the a-axis direction and further hydrogen bonds cross-link the chains.
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spelling pubmed-32752682012-02-15 Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study Eriksson, Lars Widmalm, Göran Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(24)O(10) is the methyl glycoside of a structural element α-l-Fucp-(1→ 3)-α-d-Galp making up two thirds of the repeating unit in the capsular polysaccharide of Klebsiella K63. The conformation of the title compound is described by the glycosidic torsion angles ϕ(H) = 55 (1)° and ψ(H) = −24 (1)°. The hy­droxy­methyl group in the galactose residue is present in the gauche–trans conformation. In the crystal, O—H⋯O hydrogen bonds connect the disaccharide units into chains along the a-axis direction and further hydrogen bonds cross-link the chains. International Union of Crystallography 2012-01-31 /pmc/articles/PMC3275268/ /pubmed/22347124 http://dx.doi.org/10.1107/S1600536812002279 Text en © Eriksson and Widmalm 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Eriksson, Lars
Widmalm, Göran
Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study
title Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study
title_full Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study
title_fullStr Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study
title_full_unstemmed Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study
title_short Methyl 3-O-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study
title_sort methyl 3-o-α-l-fucopyranosyl α-d-gal­acto­pyran­oside: a synchrotron study
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275268/
https://www.ncbi.nlm.nih.gov/pubmed/22347124
http://dx.doi.org/10.1107/S1600536812002279
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