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Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose
The title compound, C(8)H(12)O(6), was synthesized by deacetylation of 6-acetyl-1,2,3,4-di-O-methylene-α-d-galactose with sodium methoxide. The central part of the molecule consists of a six-membered C(5)O pyranose ring with a twist-boat conformation. Both fused dioxolane rings adopt an envelop...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719923/ https://www.ncbi.nlm.nih.gov/pubmed/26870551 http://dx.doi.org/10.1107/S2056989015021854 |
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author | Tiritiris, Ioannis Tussetschläger, Stefan Kantlehner, Willi |
author_facet | Tiritiris, Ioannis Tussetschläger, Stefan Kantlehner, Willi |
author_sort | Tiritiris, Ioannis |
collection | PubMed |
description | The title compound, C(8)H(12)O(6), was synthesized by deacetylation of 6-acetyl-1,2,3,4-di-O-methylene-α-d-galactose with sodium methoxide. The central part of the molecule consists of a six-membered C(5)O pyranose ring with a twist-boat conformation. Both fused dioxolane rings adopt an envelope conformation with C and O atoms as the flap. In the crystal, O—H⋯O and C—H⋯O hydrogen bonds are present between adjacent molecules, generating a three-dimensional network. |
format | Online Article Text |
id | pubmed-4719923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-47199232016-02-11 Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose Tiritiris, Ioannis Tussetschläger, Stefan Kantlehner, Willi Acta Crystallogr E Crystallogr Commun Data Reports The title compound, C(8)H(12)O(6), was synthesized by deacetylation of 6-acetyl-1,2,3,4-di-O-methylene-α-d-galactose with sodium methoxide. The central part of the molecule consists of a six-membered C(5)O pyranose ring with a twist-boat conformation. Both fused dioxolane rings adopt an envelope conformation with C and O atoms as the flap. In the crystal, O—H⋯O and C—H⋯O hydrogen bonds are present between adjacent molecules, generating a three-dimensional network. International Union of Crystallography 2015-11-21 /pmc/articles/PMC4719923/ /pubmed/26870551 http://dx.doi.org/10.1107/S2056989015021854 Text en © Tiritiris et al. 2015 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 | Data Reports Tiritiris, Ioannis Tussetschläger, Stefan Kantlehner, Willi Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose |
title | Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose |
title_full | Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose |
title_fullStr | Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose |
title_full_unstemmed | Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose |
title_short | Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose |
title_sort | crystal structure of 1,2,3,4-di-o-methylene-α-d-galactopyranose |
topic | Data Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719923/ https://www.ncbi.nlm.nih.gov/pubmed/26870551 http://dx.doi.org/10.1107/S2056989015021854 |
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