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3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose
The title compound, C(24)H(27)NO(9), is one of the epimers of the Henry reaction of 3-O-benzyl-6-O-benzoyl-2-O-isopropylidene-a-d-glucofuran-5-one with nitromethane. The conformation of the five membered rings is as expected from the precursor compound and the molecule is folded with a dihedral a...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968333/ https://www.ncbi.nlm.nih.gov/pubmed/21581936 http://dx.doi.org/10.1107/S1600536808043353 |
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author | Pampín, Begoña Valencia, Laura Estévez, Juan C. Estévez, Ramón J. |
author_facet | Pampín, Begoña Valencia, Laura Estévez, Juan C. Estévez, Ramón J. |
author_sort | Pampín, Begoña |
collection | PubMed |
description | The title compound, C(24)H(27)NO(9), is one of the epimers of the Henry reaction of 3-O-benzyl-6-O-benzoyl-2-O-isopropylidene-a-d-glucofuran-5-one with nitromethane. The conformation of the five membered rings is as expected from the precursor compound and the molecule is folded with a dihedral angle of 51.4 (2)° between the aromatic rings. One O—H⋯O hydrogen bond and some intramolecular and intermolecular C—H⋯O interactions are observed in the structure. |
format | Text |
id | pubmed-2968333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29683332010-12-30 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose Pampín, Begoña Valencia, Laura Estévez, Juan C. Estévez, Ramón J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(27)NO(9), is one of the epimers of the Henry reaction of 3-O-benzyl-6-O-benzoyl-2-O-isopropylidene-a-d-glucofuran-5-one with nitromethane. The conformation of the five membered rings is as expected from the precursor compound and the molecule is folded with a dihedral angle of 51.4 (2)° between the aromatic rings. One O—H⋯O hydrogen bond and some intramolecular and intermolecular C—H⋯O interactions are observed in the structure. International Union of Crystallography 2009-01-17 /pmc/articles/PMC2968333/ /pubmed/21581936 http://dx.doi.org/10.1107/S1600536808043353 Text en © Pampín et al. 2009 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 Pampín, Begoña Valencia, Laura Estévez, Juan C. Estévez, Ramón J. 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose |
title | 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose |
title_full | 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose |
title_fullStr | 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose |
title_full_unstemmed | 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose |
title_short | 3-O-Benzyl-6-O-benzoyl-1,2-O-isopropilidene-5-C-nitromethyl-a-d-glucofuranose |
title_sort | 3-o-benzyl-6-o-benzoyl-1,2-o-isopropilidene-5-c-nitromethyl-a-d-glucofuranose |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968333/ https://www.ncbi.nlm.nih.gov/pubmed/21581936 http://dx.doi.org/10.1107/S1600536808043353 |
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