2-De­oxy-α-d-arabino-hexopyran­ose

The title compound, C(6)H(12)O(5), is the α-pyran­ose form of the reducing aldose 2-de­oxy-d-arabino-hexose. The six-membered pyran­ose ring adopts a (4) C (1) conformation, with the anomeric hy­droxy group in axial and the other substituents in equatorial positions. In the crystal, each of the four...

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Detalles Bibliográficos
Autores principales: Hess, David, Klüfers, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201514/
https://www.ncbi.nlm.nih.gov/pubmed/22058760
http://dx.doi.org/10.1107/S1600536811035264
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author Hess, David
Klüfers, Peter
author_facet Hess, David
Klüfers, Peter
author_sort Hess, David
collection PubMed
description The title compound, C(6)H(12)O(5), is the α-pyran­ose form of the reducing aldose 2-de­oxy-d-arabino-hexose. The six-membered pyran­ose ring adopts a (4) C (1) conformation, with the anomeric hy­droxy group in axial and the other substituents in equatorial positions. In the crystal, each of the four hy­droxy groups acts as an inter­molecular hydrogen-bond donor function, resulting in a three-dimensional hydrogen-bonded network.
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spelling pubmed-32015142011-11-06 2-De­oxy-α-d-arabino-hexopyran­ose Hess, David Klüfers, Peter Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(6)H(12)O(5), is the α-pyran­ose form of the reducing aldose 2-de­oxy-d-arabino-hexose. The six-membered pyran­ose ring adopts a (4) C (1) conformation, with the anomeric hy­droxy group in axial and the other substituents in equatorial positions. In the crystal, each of the four hy­droxy groups acts as an inter­molecular hydrogen-bond donor function, resulting in a three-dimensional hydrogen-bonded network. International Union of Crystallography 2011-09-14 /pmc/articles/PMC3201514/ /pubmed/22058760 http://dx.doi.org/10.1107/S1600536811035264 Text en © Hess and Klüfers 2011 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
Hess, David
Klüfers, Peter
2-De­oxy-α-d-arabino-hexopyran­ose
title 2-De­oxy-α-d-arabino-hexopyran­ose
title_full 2-De­oxy-α-d-arabino-hexopyran­ose
title_fullStr 2-De­oxy-α-d-arabino-hexopyran­ose
title_full_unstemmed 2-De­oxy-α-d-arabino-hexopyran­ose
title_short 2-De­oxy-α-d-arabino-hexopyran­ose
title_sort 2-de­oxy-α-d-arabino-hexopyran­ose
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201514/
https://www.ncbi.nlm.nih.gov/pubmed/22058760
http://dx.doi.org/10.1107/S1600536811035264
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