4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside

The enanti­omerically pure title compound, C(23)H(30)O(12), crystallizes in the chiral space group P2(1)2(1)2(1). The O-acetyl­ated-glucopyran­oside moiety adopts a chair conformation. Numerous C—H⋯O inter­actions as well as a C—H⋯π inter­action are present in the crystal structure.

Detalles Bibliográficos
Autores principales: Zipp, Caitlin F., Fernandes, Manuel, Marques, Helder M., Michael, Joseph P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344139/
https://www.ncbi.nlm.nih.gov/pubmed/22606142
http://dx.doi.org/10.1107/S160053681201121X
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author Zipp, Caitlin F.
Fernandes, Manuel
Marques, Helder M.
Michael, Joseph P.
author_facet Zipp, Caitlin F.
Fernandes, Manuel
Marques, Helder M.
Michael, Joseph P.
author_sort Zipp, Caitlin F.
collection PubMed
description The enanti­omerically pure title compound, C(23)H(30)O(12), crystallizes in the chiral space group P2(1)2(1)2(1). The O-acetyl­ated-glucopyran­oside moiety adopts a chair conformation. Numerous C—H⋯O inter­actions as well as a C—H⋯π inter­action are present in the crystal structure.
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spelling pubmed-33441392012-05-17 4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside Zipp, Caitlin F. Fernandes, Manuel Marques, Helder M. Michael, Joseph P. Acta Crystallogr Sect E Struct Rep Online Organic Papers The enanti­omerically pure title compound, C(23)H(30)O(12), crystallizes in the chiral space group P2(1)2(1)2(1). The O-acetyl­ated-glucopyran­oside moiety adopts a chair conformation. Numerous C—H⋯O inter­actions as well as a C—H⋯π inter­action are present in the crystal structure. International Union of Crystallography 2012-03-28 /pmc/articles/PMC3344139/ /pubmed/22606142 http://dx.doi.org/10.1107/S160053681201121X Text en © Zipp 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
Zipp, Caitlin F.
Fernandes, Manuel
Marques, Helder M.
Michael, Joseph P.
4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title 4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_full 4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_fullStr 4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_full_unstemmed 4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_short 4-(Dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside
title_sort 4-(dimeth­oxy­meth­yl)phenyl 2,3,4,6-tetra-o-acetyl-β-d-glucopyran­oside
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344139/
https://www.ncbi.nlm.nih.gov/pubmed/22606142
http://dx.doi.org/10.1107/S160053681201121X
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