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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)...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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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. |
format | Online Article Text |
id | pubmed-3275268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT erikssonlars methyl3oalfucopyranosyladgalactopyranosideasynchrotronstudy AT widmalmgoran methyl3oalfucopyranosyladgalactopyranosideasynchrotronstudy |