4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside

The pyran­oside ring in the title compound, C(21)H(24)O(11), has a chair conformation with the substituted benzene ring occupying an equatorial position. The crystal packing is dominated by C—H⋯O inter­actions that lead to the formation of supra­molecular layers in the ab plane.

Detalles Bibliográficos
Autores principales: Heidelberg, Thorsten, Hussen, Rusnah Syahila Duali, Rodzi, Nasrul Zamani Mohd, Ng, Seik Weng, Tiekink, Edward R. T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099765/
https://www.ncbi.nlm.nih.gov/pubmed/21754109
http://dx.doi.org/10.1107/S1600536811008099
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author Heidelberg, Thorsten
Hussen, Rusnah Syahila Duali
Rodzi, Nasrul Zamani Mohd
Ng, Seik Weng
Tiekink, Edward R. T.
author_facet Heidelberg, Thorsten
Hussen, Rusnah Syahila Duali
Rodzi, Nasrul Zamani Mohd
Ng, Seik Weng
Tiekink, Edward R. T.
author_sort Heidelberg, Thorsten
collection PubMed
description The pyran­oside ring in the title compound, C(21)H(24)O(11), has a chair conformation with the substituted benzene ring occupying an equatorial position. The crystal packing is dominated by C—H⋯O inter­actions that lead to the formation of supra­molecular layers in the ab plane.
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spelling pubmed-30997652011-07-13 4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside Heidelberg, Thorsten Hussen, Rusnah Syahila Duali Rodzi, Nasrul Zamani Mohd Ng, Seik Weng Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The pyran­oside ring in the title compound, C(21)H(24)O(11), has a chair conformation with the substituted benzene ring occupying an equatorial position. The crystal packing is dominated by C—H⋯O inter­actions that lead to the formation of supra­molecular layers in the ab plane. International Union of Crystallography 2011-03-09 /pmc/articles/PMC3099765/ /pubmed/21754109 http://dx.doi.org/10.1107/S1600536811008099 Text en © Heidelberg et al. 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
Heidelberg, Thorsten
Hussen, Rusnah Syahila Duali
Rodzi, Nasrul Zamani Mohd
Ng, Seik Weng
Tiekink, Edward R. T.
4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title 4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_full 4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_fullStr 4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_full_unstemmed 4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_short 4-Formyl­phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_sort 4-formyl­phenyl 2,3,4,6-tetra-o-acetyl-β-d-glucopyran­oside
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099765/
https://www.ncbi.nlm.nih.gov/pubmed/21754109
http://dx.doi.org/10.1107/S1600536811008099
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