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6-Deoxy-α-l-talopyranose
X-ray crystallography showed that the title compound, C(6)H(12)O(5), crystallizes in the α-pyranose form with the six-membered ring in a chair conformation. The crystal structure exists as a three-dimensional hydrogen-bonded network of molecules with each molecule acting as a donor and aceptor fo...
| Autores principales: | , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962018/ https://www.ncbi.nlm.nih.gov/pubmed/21203105 http://dx.doi.org/10.1107/S1600536808019582 |
| _version_ | 1782189121236631552 |
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| author | Booth, K. Victoria Jenkinson, Sarah F. Fleet, George W. J. Gullapalli, Pushpakiran Yoshihara, Akihide Izumori, Ken Watkin, David J. |
| author_facet | Booth, K. Victoria Jenkinson, Sarah F. Fleet, George W. J. Gullapalli, Pushpakiran Yoshihara, Akihide Izumori, Ken Watkin, David J. |
| author_sort | Booth, K. Victoria |
| collection | PubMed |
| description | X-ray crystallography showed that the title compound, C(6)H(12)O(5), crystallizes in the α-pyranose form with the six-membered ring in a chair conformation. The crystal structure exists as a three-dimensional hydrogen-bonded network of molecules with each molecule acting as a donor and aceptor for four hydrogen bonds. The absolute configuration was determined by the use of l-fucose as starting material. |
| format | Text |
| id | pubmed-2962018 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2008 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29620182010-12-30 6-Deoxy-α-l-talopyranose Booth, K. Victoria Jenkinson, Sarah F. Fleet, George W. J. Gullapalli, Pushpakiran Yoshihara, Akihide Izumori, Ken Watkin, David J. Acta Crystallogr Sect E Struct Rep Online Organic Papers X-ray crystallography showed that the title compound, C(6)H(12)O(5), crystallizes in the α-pyranose form with the six-membered ring in a chair conformation. The crystal structure exists as a three-dimensional hydrogen-bonded network of molecules with each molecule acting as a donor and aceptor for four hydrogen bonds. The absolute configuration was determined by the use of l-fucose as starting material. International Union of Crystallography 2008-07-05 /pmc/articles/PMC2962018/ /pubmed/21203105 http://dx.doi.org/10.1107/S1600536808019582 Text en © Booth et al. 2008 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 Booth, K. Victoria Jenkinson, Sarah F. Fleet, George W. J. Gullapalli, Pushpakiran Yoshihara, Akihide Izumori, Ken Watkin, David J. 6-Deoxy-α-l-talopyranose |
| title | 6-Deoxy-α-l-talopyranose |
| title_full | 6-Deoxy-α-l-talopyranose |
| title_fullStr | 6-Deoxy-α-l-talopyranose |
| title_full_unstemmed | 6-Deoxy-α-l-talopyranose |
| title_short | 6-Deoxy-α-l-talopyranose |
| title_sort | 6-deoxy-α-l-talopyranose |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962018/ https://www.ncbi.nlm.nih.gov/pubmed/21203105 http://dx.doi.org/10.1107/S1600536808019582 |
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