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Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate
The title compound, 3C(7)H(10)O(6)·H(2)O, is the enantiomerically pure product of a multi-step synthesis from the enantiomerically pure natural shikimic acid. The asymmetric unit contains three molecules of the acid and one molecule of water. The cyclohexene rings of the acids have half-chair c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515248/ https://www.ncbi.nlm.nih.gov/pubmed/23284468 http://dx.doi.org/10.1107/S1600536812041256 |
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author | Griesbeck, Axel G. Miara, Claus Neudörfl, Jörg-M. |
author_facet | Griesbeck, Axel G. Miara, Claus Neudörfl, Jörg-M. |
author_sort | Griesbeck, Axel G. |
collection | PubMed |
description | The title compound, 3C(7)H(10)O(6)·H(2)O, is the enantiomerically pure product of a multi-step synthesis from the enantiomerically pure natural shikimic acid. The asymmetric unit contains three molecules of the acid and one molecule of water. The cyclohexene rings of the acids have half-chair conformations. The carboxylate, the four hydroxide groups and the additional water molecule form a complex three-dimensional hydrogen-bonding network. |
format | Online Article Text |
id | pubmed-3515248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35152482013-01-02 Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate Griesbeck, Axel G. Miara, Claus Neudörfl, Jörg-M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, 3C(7)H(10)O(6)·H(2)O, is the enantiomerically pure product of a multi-step synthesis from the enantiomerically pure natural shikimic acid. The asymmetric unit contains three molecules of the acid and one molecule of water. The cyclohexene rings of the acids have half-chair conformations. The carboxylate, the four hydroxide groups and the additional water molecule form a complex three-dimensional hydrogen-bonding network. International Union of Crystallography 2012-10-20 /pmc/articles/PMC3515248/ /pubmed/23284468 http://dx.doi.org/10.1107/S1600536812041256 Text en © Griesbeck et al. 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 Griesbeck, Axel G. Miara, Claus Neudörfl, Jörg-M. Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate |
title | Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate |
title_full | Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate |
title_fullStr | Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate |
title_full_unstemmed | Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate |
title_short | Tris[(6S)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate |
title_sort | tris[(6s)-6-hydroxy-4-epi-shikimic acid] monohydrate: an enantiomerically pure hydroxylated shikimic acid derived from methyl shikimate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515248/ https://www.ncbi.nlm.nih.gov/pubmed/23284468 http://dx.doi.org/10.1107/S1600536812041256 |
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