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(2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one
In the title compound C(22)H(24)O(2), the exocyclic C=C double bond is in an E configuration and the tert-butyl group is in an axial position on the cyclohexanone ring. The cyclohexanone ring in the dihydronaphthalene fused-ring system adopts a half-chair conformation in both independent two mo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151781/ https://www.ncbi.nlm.nih.gov/pubmed/21837196 http://dx.doi.org/10.1107/S1600536811021969 |
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author | Akhazzane, Mohamed Zouihri, Hafid Daoudi, Maria Kerbal, Abdelali Al Houari, Ghali |
author_facet | Akhazzane, Mohamed Zouihri, Hafid Daoudi, Maria Kerbal, Abdelali Al Houari, Ghali |
author_sort | Akhazzane, Mohamed |
collection | PubMed |
description | In the title compound C(22)H(24)O(2), the exocyclic C=C double bond is in an E configuration and the tert-butyl group is in an axial position on the cyclohexanone ring. The cyclohexanone ring in the dihydronaphthalene fused-ring system adopts a half-chair conformation in both independent two molecules in the asymetric unit. The benzene ring system is oriented angles of 43.97 (12) and 39.24 (12)° with respect to the naphthyl ring system in the two independent molecules. In the crystal, molecules are linked via C—H⋯O hydrogen bonds and C—H⋯π interactions. |
format | Online Article Text |
id | pubmed-3151781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-31517812011-08-11 (2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one Akhazzane, Mohamed Zouihri, Hafid Daoudi, Maria Kerbal, Abdelali Al Houari, Ghali Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound C(22)H(24)O(2), the exocyclic C=C double bond is in an E configuration and the tert-butyl group is in an axial position on the cyclohexanone ring. The cyclohexanone ring in the dihydronaphthalene fused-ring system adopts a half-chair conformation in both independent two molecules in the asymetric unit. The benzene ring system is oriented angles of 43.97 (12) and 39.24 (12)° with respect to the naphthyl ring system in the two independent molecules. In the crystal, molecules are linked via C—H⋯O hydrogen bonds and C—H⋯π interactions. International Union of Crystallography 2011-06-25 /pmc/articles/PMC3151781/ /pubmed/21837196 http://dx.doi.org/10.1107/S1600536811021969 Text en © Akhazzane 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 Akhazzane, Mohamed Zouihri, Hafid Daoudi, Maria Kerbal, Abdelali Al Houari, Ghali (2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one |
title | (2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one |
title_full | (2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one |
title_fullStr | (2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one |
title_full_unstemmed | (2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one |
title_short | (2E)-4-tert-Butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2H)-one |
title_sort | (2e)-4-tert-butyl-2-(4-methoxybenzylidene)-3,4-dihydronaphthalen-1(2h)-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151781/ https://www.ncbi.nlm.nih.gov/pubmed/21837196 http://dx.doi.org/10.1107/S1600536811021969 |
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