(E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)

In the title compound, C(21)H(21)NO(6), each of the cyclo­hexenone rings adopts a half-chair conformation. Each of the pairs of hy­droxy and carbonyl O atoms are oriented to allow for the formation of intra­molecular O—H⋯O hydrogen bonds, which are typical of xanthene derivatives.

Detalles Bibliográficos
Autores principales: Cha, Joo Hwan, Kim, Young Hee, Lee, Jae Kyun, Cho, Yong Seo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254576/
https://www.ncbi.nlm.nih.gov/pubmed/22259527
http://dx.doi.org/10.1107/S1600536811054730
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author Cha, Joo Hwan
Kim, Young Hee
Lee, Jae Kyun
Cho, Yong Seo
author_facet Cha, Joo Hwan
Kim, Young Hee
Lee, Jae Kyun
Cho, Yong Seo
author_sort Cha, Joo Hwan
collection PubMed
description In the title compound, C(21)H(21)NO(6), each of the cyclo­hexenone rings adopts a half-chair conformation. Each of the pairs of hy­droxy and carbonyl O atoms are oriented to allow for the formation of intra­molecular O—H⋯O hydrogen bonds, which are typical of xanthene derivatives.
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spelling pubmed-32545762012-01-18 (E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one) Cha, Joo Hwan Kim, Young Hee Lee, Jae Kyun Cho, Yong Seo Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(21)NO(6), each of the cyclo­hexenone rings adopts a half-chair conformation. Each of the pairs of hy­droxy and carbonyl O atoms are oriented to allow for the formation of intra­molecular O—H⋯O hydrogen bonds, which are typical of xanthene derivatives. International Union of Crystallography 2011-12-23 /pmc/articles/PMC3254576/ /pubmed/22259527 http://dx.doi.org/10.1107/S1600536811054730 Text en © Cha et al. 2012 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
Cha, Joo Hwan
Kim, Young Hee
Lee, Jae Kyun
Cho, Yong Seo
(E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)
title (E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)
title_full (E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)
title_fullStr (E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)
title_full_unstemmed (E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)
title_short (E)-2,2′-[3-(2-Nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)
title_sort (e)-2,2′-[3-(2-nitro­phen­yl)prop-2-ene-1,1-di­yl]bis­(3-hy­droxy­cyclo­hex-2-en-1-one)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254576/
https://www.ncbi.nlm.nih.gov/pubmed/22259527
http://dx.doi.org/10.1107/S1600536811054730
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