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Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate
The title compound, C(16)H(20)O(5), was synthesized from ilicic acid [2-(8-hydroxy-4a,8-dimethyldecahydronaphthalen-2-yl)acrylic acid], which was isolated from the chloroform extract of the aerial part of Inula viscose (L) Aiton [or Dittrichia viscosa (L) Greuter]. The molecule is built up fro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275064/ https://www.ncbi.nlm.nih.gov/pubmed/22347009 http://dx.doi.org/10.1107/S1600536812000086 |
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author | Tebbaa, Mohamed Benharref, Ahmed Daran, Jean Claude Mellouki, Fouad Berraho, Moha |
author_facet | Tebbaa, Mohamed Benharref, Ahmed Daran, Jean Claude Mellouki, Fouad Berraho, Moha |
author_sort | Tebbaa, Mohamed |
collection | PubMed |
description | The title compound, C(16)H(20)O(5), was synthesized from ilicic acid [2-(8-hydroxy-4a,8-dimethyldecahydronaphthalen-2-yl)acrylic acid], which was isolated from the chloroform extract of the aerial part of Inula viscose (L) Aiton [or Dittrichia viscosa (L) Greuter]. The molecule is built up from two fused six-membered rings, the epoxidized six-membered ring adopts a half-chair conformation while the other ring displays a perfect chair conformation. The crystal structure features C—H⋯O hydrogen bonds. |
format | Online Article Text |
id | pubmed-3275064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32750642012-02-15 Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate Tebbaa, Mohamed Benharref, Ahmed Daran, Jean Claude Mellouki, Fouad Berraho, Moha Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(20)O(5), was synthesized from ilicic acid [2-(8-hydroxy-4a,8-dimethyldecahydronaphthalen-2-yl)acrylic acid], which was isolated from the chloroform extract of the aerial part of Inula viscose (L) Aiton [or Dittrichia viscosa (L) Greuter]. The molecule is built up from two fused six-membered rings, the epoxidized six-membered ring adopts a half-chair conformation while the other ring displays a perfect chair conformation. The crystal structure features C—H⋯O hydrogen bonds. International Union of Crystallography 2012-01-14 /pmc/articles/PMC3275064/ /pubmed/22347009 http://dx.doi.org/10.1107/S1600536812000086 Text en © Tebbaa 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 Tebbaa, Mohamed Benharref, Ahmed Daran, Jean Claude Mellouki, Fouad Berraho, Moha Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate |
title | Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate |
title_full | Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate |
title_fullStr | Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate |
title_full_unstemmed | Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate |
title_short | Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1aH-1-oxacyclopropa[d]naphthalen-7-yl)acrylate |
title_sort | methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octahydro-1ah-1-oxacyclopropa[d]naphthalen-7-yl)acrylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275064/ https://www.ncbi.nlm.nih.gov/pubmed/22347009 http://dx.doi.org/10.1107/S1600536812000086 |
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