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2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)

In the title mol­ecule, C(25)H(30)O(4), the two cyclo­hexene rings adopt envelope conformations. The two hy­droxy groups are involved in the formation of intra­molecular O—H⋯O hydrogen bonds. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules related by translation a...

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Detalles Bibliográficos
Autores principales: Zhu, Yu-Lin, Xiao, Guo-Lan, Chen, Yan-Fen, Chen, Rui-Ting, Zhou, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200888/
https://www.ncbi.nlm.nih.gov/pubmed/22065510
http://dx.doi.org/10.1107/S1600536811033745
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author Zhu, Yu-Lin
Xiao, Guo-Lan
Chen, Yan-Fen
Chen, Rui-Ting
Zhou, Ying
author_facet Zhu, Yu-Lin
Xiao, Guo-Lan
Chen, Yan-Fen
Chen, Rui-Ting
Zhou, Ying
author_sort Zhu, Yu-Lin
collection PubMed
description In the title mol­ecule, C(25)H(30)O(4), the two cyclo­hexene rings adopt envelope conformations. The two hy­droxy groups are involved in the formation of intra­molecular O—H⋯O hydrogen bonds. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules related by translation along the axis a into chains.
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spelling pubmed-32008882011-11-06 2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one) Zhu, Yu-Lin Xiao, Guo-Lan Chen, Yan-Fen Chen, Rui-Ting Zhou, Ying Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(25)H(30)O(4), the two cyclo­hexene rings adopt envelope conformations. The two hy­droxy groups are involved in the formation of intra­molecular O—H⋯O hydrogen bonds. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules related by translation along the axis a into chains. International Union of Crystallography 2011-08-27 /pmc/articles/PMC3200888/ /pubmed/22065510 http://dx.doi.org/10.1107/S1600536811033745 Text en © Zhu 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
Zhu, Yu-Lin
Xiao, Guo-Lan
Chen, Yan-Fen
Chen, Rui-Ting
Zhou, Ying
2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)
title 2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)
title_full 2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)
title_fullStr 2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)
title_full_unstemmed 2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)
title_short 2,2′-[(1E)-3-Phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)
title_sort 2,2′-[(1e)-3-phenyl­prop-2-ene-1,1-di­yl]bis­(3-hy­droxy-5,5-dimethyl­cyclo­hex-2-en-1-one)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200888/
https://www.ncbi.nlm.nih.gov/pubmed/22065510
http://dx.doi.org/10.1107/S1600536811033745
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