(3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one

The piperidine ring in the title compound, C(24)H(25)NO(3), adopts an envelope conformation with the N atom being the flap atom, and each C=C double bond exhibits an E conformation. In the crystal, C—H⋯O hydrogen bonds link the mol­ecules, forming supramolecular layers that stack along the a axis....

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Detalles Bibliográficos
Autores principales: Almansour, Abdulrahman I., Kumar, Raju Suresh, Arumugam, Natarajan, Vishnupriya, R., Suresh, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770353/
https://www.ncbi.nlm.nih.gov/pubmed/24046638
http://dx.doi.org/10.1107/S1600536813015195
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author Almansour, Abdulrahman I.
Kumar, Raju Suresh
Arumugam, Natarajan
Vishnupriya, R.
Suresh, J.
author_facet Almansour, Abdulrahman I.
Kumar, Raju Suresh
Arumugam, Natarajan
Vishnupriya, R.
Suresh, J.
author_sort Almansour, Abdulrahman I.
collection PubMed
description The piperidine ring in the title compound, C(24)H(25)NO(3), adopts an envelope conformation with the N atom being the flap atom, and each C=C double bond exhibits an E conformation. In the crystal, C—H⋯O hydrogen bonds link the mol­ecules, forming supramolecular layers that stack along the a axis.
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spelling pubmed-37703532013-09-17 (3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one Almansour, Abdulrahman I. Kumar, Raju Suresh Arumugam, Natarajan Vishnupriya, R. Suresh, J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The piperidine ring in the title compound, C(24)H(25)NO(3), adopts an envelope conformation with the N atom being the flap atom, and each C=C double bond exhibits an E conformation. In the crystal, C—H⋯O hydrogen bonds link the mol­ecules, forming supramolecular layers that stack along the a axis. International Union of Crystallography 2013-06-12 /pmc/articles/PMC3770353/ /pubmed/24046638 http://dx.doi.org/10.1107/S1600536813015195 Text en © Almansour et al. 2013 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
Almansour, Abdulrahman I.
Kumar, Raju Suresh
Arumugam, Natarajan
Vishnupriya, R.
Suresh, J.
(3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one
title (3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one
title_full (3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one
title_fullStr (3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one
title_full_unstemmed (3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one
title_short (3E,5E)-1-Allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one
title_sort (3e,5e)-1-allyl-3,5-bis(4-meth­oxy­benzyl­idene)­piperidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770353/
https://www.ncbi.nlm.nih.gov/pubmed/24046638
http://dx.doi.org/10.1107/S1600536813015195
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