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(2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none

The title compound, C(25)H(28)O(7), was prepared by the base-catalysed reaction of 3,4,5-trimethoxy­benzaldehyde with cyclo­penta­none. The mol­ecule has crystallographic twofold rotation symmetry and adopts an E-configuration about the central olefinic bonds. The two benzene rings and the central c...

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Detalles Bibliográficos
Autores principales: Sun, Yi-Feng, Liu, Yang, Zhang, Feng-Yu, Chen, Hong-Ji, Cui, Yi-Ping
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959310/
https://www.ncbi.nlm.nih.gov/pubmed/21201165
http://dx.doi.org/10.1107/S1600536808029474
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author Sun, Yi-Feng
Liu, Yang
Zhang, Feng-Yu
Chen, Hong-Ji
Cui, Yi-Ping
author_facet Sun, Yi-Feng
Liu, Yang
Zhang, Feng-Yu
Chen, Hong-Ji
Cui, Yi-Ping
author_sort Sun, Yi-Feng
collection PubMed
description The title compound, C(25)H(28)O(7), was prepared by the base-catalysed reaction of 3,4,5-trimethoxy­benzaldehyde with cyclo­penta­none. The mol­ecule has crystallographic twofold rotation symmetry and adopts an E-configuration about the central olefinic bonds. The two benzene rings and the central cyclo­penta­none ring are almost coplanar [dihedral angle = 4.7 (2)°].
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spelling pubmed-29593102010-12-30 (2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none Sun, Yi-Feng Liu, Yang Zhang, Feng-Yu Chen, Hong-Ji Cui, Yi-Ping Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(25)H(28)O(7), was prepared by the base-catalysed reaction of 3,4,5-trimethoxy­benzaldehyde with cyclo­penta­none. The mol­ecule has crystallographic twofold rotation symmetry and adopts an E-configuration about the central olefinic bonds. The two benzene rings and the central cyclo­penta­none ring are almost coplanar [dihedral angle = 4.7 (2)°]. International Union of Crystallography 2008-09-20 /pmc/articles/PMC2959310/ /pubmed/21201165 http://dx.doi.org/10.1107/S1600536808029474 Text en © Sun et al. 2008 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
Sun, Yi-Feng
Liu, Yang
Zhang, Feng-Yu
Chen, Hong-Ji
Cui, Yi-Ping
(2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none
title (2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none
title_full (2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none
title_fullStr (2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none
title_full_unstemmed (2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none
title_short (2E,5E)-2,5-Bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none
title_sort (2e,5e)-2,5-bis(3,4,5-trimethoxy­benzyl­idene)cyclo­penta­none
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959310/
https://www.ncbi.nlm.nih.gov/pubmed/21201165
http://dx.doi.org/10.1107/S1600536808029474
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