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Crystal structure of tetrahydroseselin, an angular pyranocoumarin
In the title compound, tetrahydroseselin, C(14)H(16)O(3), a pyranocoumarin [systematic name: 8,8-dimethyl-3,4,9,10-tetrahydro-2H,8H-pyrano[2,3-f]chromen-2-one] obtained from the hydrogenation of seselin in the presence of Pd/C in MeOH at room temperature, the dihedral angle between the central b...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598830/ https://www.ncbi.nlm.nih.gov/pubmed/28932418 http://dx.doi.org/10.1107/S205698901700932X |
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author | Bauri, A. K. Foro, S. Rahman, A. F. M. M. |
author_facet | Bauri, A. K. Foro, S. Rahman, A. F. M. M. |
author_sort | Bauri, A. K. |
collection | PubMed |
description | In the title compound, tetrahydroseselin, C(14)H(16)O(3), a pyranocoumarin [systematic name: 8,8-dimethyl-3,4,9,10-tetrahydro-2H,8H-pyrano[2,3-f]chromen-2-one] obtained from the hydrogenation of seselin in the presence of Pd/C in MeOH at room temperature, the dihedral angle between the central benzene ring and the best planes of the outer fused ring systems are 6.20 (7) and 10.02 (8)°. In the crystal, molecules show only very weak intermolecular C—H⋯O interactions. |
format | Online Article Text |
id | pubmed-5598830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-55988302017-09-20 Crystal structure of tetrahydroseselin, an angular pyranocoumarin Bauri, A. K. Foro, S. Rahman, A. F. M. M. Acta Crystallogr E Crystallogr Commun Research Communications In the title compound, tetrahydroseselin, C(14)H(16)O(3), a pyranocoumarin [systematic name: 8,8-dimethyl-3,4,9,10-tetrahydro-2H,8H-pyrano[2,3-f]chromen-2-one] obtained from the hydrogenation of seselin in the presence of Pd/C in MeOH at room temperature, the dihedral angle between the central benzene ring and the best planes of the outer fused ring systems are 6.20 (7) and 10.02 (8)°. In the crystal, molecules show only very weak intermolecular C—H⋯O interactions. International Union of Crystallography 2017-07-04 /pmc/articles/PMC5598830/ /pubmed/28932418 http://dx.doi.org/10.1107/S205698901700932X Text en © Bauri et al. 2017 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/2.0/uk/ |
spellingShingle | Research Communications Bauri, A. K. Foro, S. Rahman, A. F. M. M. Crystal structure of tetrahydroseselin, an angular pyranocoumarin |
title | Crystal structure of tetrahydroseselin, an angular pyranocoumarin |
title_full | Crystal structure of tetrahydroseselin, an angular pyranocoumarin |
title_fullStr | Crystal structure of tetrahydroseselin, an angular pyranocoumarin |
title_full_unstemmed | Crystal structure of tetrahydroseselin, an angular pyranocoumarin |
title_short | Crystal structure of tetrahydroseselin, an angular pyranocoumarin |
title_sort | crystal structure of tetrahydroseselin, an angular pyranocoumarin |
topic | Research Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598830/ https://www.ncbi.nlm.nih.gov/pubmed/28932418 http://dx.doi.org/10.1107/S205698901700932X |
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