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6-Deoxy-6-fluoro-d-galactose
The crystal structure unequivocally confirms the relative stereochemistry of the title compound, C(6)H(11)FO(5). The absolute stereochemistry was determined by the use of d-galactose as the starting material. The compound exists as a three-dimensional O—H⋯O hydrogen-bonded network with each molecul...
| Autores principales: | , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979621/ https://www.ncbi.nlm.nih.gov/pubmed/21579408 http://dx.doi.org/10.1107/S1600536810016612 |
| _version_ | 1782191456977420288 |
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| author | Jenkinson, Sarah F. Best, Daniel Izumori, Ken Wilson, Francis X. Weymouth-Wilson, Alexander C. Fleet, George W. J. Thompson, Amber L. |
| author_facet | Jenkinson, Sarah F. Best, Daniel Izumori, Ken Wilson, Francis X. Weymouth-Wilson, Alexander C. Fleet, George W. J. Thompson, Amber L. |
| author_sort | Jenkinson, Sarah F. |
| collection | PubMed |
| description | The crystal structure unequivocally confirms the relative stereochemistry of the title compound, C(6)H(11)FO(5). The absolute stereochemistry was determined by the use of d-galactose as the starting material. The compound exists as a three-dimensional O—H⋯O hydrogen-bonded network with each molecule acting as a donor and acceptor for four hydrogen bonds. |
| format | Text |
| id | pubmed-2979621 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2010 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29796212010-12-30 6-Deoxy-6-fluoro-d-galactose Jenkinson, Sarah F. Best, Daniel Izumori, Ken Wilson, Francis X. Weymouth-Wilson, Alexander C. Fleet, George W. J. Thompson, Amber L. Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure unequivocally confirms the relative stereochemistry of the title compound, C(6)H(11)FO(5). The absolute stereochemistry was determined by the use of d-galactose as the starting material. The compound exists as a three-dimensional O—H⋯O hydrogen-bonded network with each molecule acting as a donor and acceptor for four hydrogen bonds. International Union of Crystallography 2010-05-12 /pmc/articles/PMC2979621/ /pubmed/21579408 http://dx.doi.org/10.1107/S1600536810016612 Text en © Jenkinson et al. 2010 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 Jenkinson, Sarah F. Best, Daniel Izumori, Ken Wilson, Francis X. Weymouth-Wilson, Alexander C. Fleet, George W. J. Thompson, Amber L. 6-Deoxy-6-fluoro-d-galactose |
| title | 6-Deoxy-6-fluoro-d-galactose |
| title_full | 6-Deoxy-6-fluoro-d-galactose |
| title_fullStr | 6-Deoxy-6-fluoro-d-galactose |
| title_full_unstemmed | 6-Deoxy-6-fluoro-d-galactose |
| title_short | 6-Deoxy-6-fluoro-d-galactose |
| title_sort | 6-deoxy-6-fluoro-d-galactose |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979621/ https://www.ncbi.nlm.nih.gov/pubmed/21579408 http://dx.doi.org/10.1107/S1600536810016612 |
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