rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione

The title compound, C(13)H(16)O(2), is a chiral bicyclic structure composed of two fused cyclo­hexa­ne rings possessing both boat and chair conformations. The mol­ecules are packed in enantio­pure columns which are pairwise linked forming an overall racemic solid; within the column pairs the packing...

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Detalles Bibliográficos
Autores principales: Orentas, Edvinas, Wendt, Ola F., Wärnmark, Kenneth, Butkus, Eugenijus, Wallentin, Carl-Johan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969760/
https://www.ncbi.nlm.nih.gov/pubmed/21583208
http://dx.doi.org/10.1107/S1600536809018443
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author Orentas, Edvinas
Wendt, Ola F.
Wärnmark, Kenneth
Butkus, Eugenijus
Wallentin, Carl-Johan
author_facet Orentas, Edvinas
Wendt, Ola F.
Wärnmark, Kenneth
Butkus, Eugenijus
Wallentin, Carl-Johan
author_sort Orentas, Edvinas
collection PubMed
description The title compound, C(13)H(16)O(2), is a chiral bicyclic structure composed of two fused cyclo­hexa­ne rings possessing both boat and chair conformations. The mol­ecules are packed in enantio­pure columns which are pairwise linked forming an overall racemic solid; within the column pairs the packing is governed by weak dipole–dipole inter­actions stemming from stacked carbonyl functionalities (CO(centroid)–CO(centroid) distance = 3.290 Å).
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spelling pubmed-29697602010-12-30 rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione Orentas, Edvinas Wendt, Ola F. Wärnmark, Kenneth Butkus, Eugenijus Wallentin, Carl-Johan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(16)O(2), is a chiral bicyclic structure composed of two fused cyclo­hexa­ne rings possessing both boat and chair conformations. The mol­ecules are packed in enantio­pure columns which are pairwise linked forming an overall racemic solid; within the column pairs the packing is governed by weak dipole–dipole inter­actions stemming from stacked carbonyl functionalities (CO(centroid)–CO(centroid) distance = 3.290 Å). International Union of Crystallography 2009-05-20 /pmc/articles/PMC2969760/ /pubmed/21583208 http://dx.doi.org/10.1107/S1600536809018443 Text en © Orentas 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
Orentas, Edvinas
Wendt, Ola F.
Wärnmark, Kenneth
Butkus, Eugenijus
Wallentin, Carl-Johan
rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione
title rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione
title_full rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione
title_fullStr rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione
title_full_unstemmed rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione
title_short rac-4,8-Divinyl­bicyclo­[3.3.1]nonane-2,6-dione
title_sort rac-4,8-divinyl­bicyclo­[3.3.1]nonane-2,6-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969760/
https://www.ncbi.nlm.nih.gov/pubmed/21583208
http://dx.doi.org/10.1107/S1600536809018443
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