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β-d-Altrose
The molecule of the title compound, C(6)H(12)O(6), [systematic name: (2R,3S,4R,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol] adopts a (4) C (1) chair conformation with the anomeric hydroxyl group in the equatorial position. All hydroxyl groups act as donors and acceptors in hydrogen bonding and t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968302/ https://www.ncbi.nlm.nih.gov/pubmed/21581893 http://dx.doi.org/10.1107/S1600536809000397 |
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author | Watanabe, Yuji Yoshida, Hiromi Takeda, Kosei Ishi, Tomohiko Kamitori, Shigehiro |
author_facet | Watanabe, Yuji Yoshida, Hiromi Takeda, Kosei Ishi, Tomohiko Kamitori, Shigehiro |
author_sort | Watanabe, Yuji |
collection | PubMed |
description | The molecule of the title compound, C(6)H(12)O(6), [systematic name: (2R,3S,4R,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol] adopts a (4) C (1) chair conformation with the anomeric hydroxyl group in the equatorial position. All hydroxyl groups act as donors and acceptors in hydrogen bonding and the molecule is involved in ten intermolecular O—H⋯O interactions [O⋯O = 2.672 (5)–2.776 (4) Å] with eight neighbouring molecules. Two independent O—H⋯O—H⋯ helices extending along the z axis are found in this structure. |
format | Text |
id | pubmed-2968302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29683022010-12-30 β-d-Altrose Watanabe, Yuji Yoshida, Hiromi Takeda, Kosei Ishi, Tomohiko Kamitori, Shigehiro Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecule of the title compound, C(6)H(12)O(6), [systematic name: (2R,3S,4R,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol] adopts a (4) C (1) chair conformation with the anomeric hydroxyl group in the equatorial position. All hydroxyl groups act as donors and acceptors in hydrogen bonding and the molecule is involved in ten intermolecular O—H⋯O interactions [O⋯O = 2.672 (5)–2.776 (4) Å] with eight neighbouring molecules. Two independent O—H⋯O—H⋯ helices extending along the z axis are found in this structure. International Union of Crystallography 2009-01-10 /pmc/articles/PMC2968302/ /pubmed/21581893 http://dx.doi.org/10.1107/S1600536809000397 Text en © Watanabe et al. 2009 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 Watanabe, Yuji Yoshida, Hiromi Takeda, Kosei Ishi, Tomohiko Kamitori, Shigehiro β-d-Altrose |
title | β-d-Altrose |
title_full | β-d-Altrose |
title_fullStr | β-d-Altrose |
title_full_unstemmed | β-d-Altrose |
title_short | β-d-Altrose |
title_sort | β-d-altrose |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968302/ https://www.ncbi.nlm.nih.gov/pubmed/21581893 http://dx.doi.org/10.1107/S1600536809000397 |
work_keys_str_mv | AT watanabeyuji bdaltrose AT yoshidahiromi bdaltrose AT takedakosei bdaltrose AT ishitomohiko bdaltrose AT kamitorishigehiro bdaltrose |