Cargando…
3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one
In the title compound, C(22)H(24)O(5), each of the cyclohexenone rings adopts a half-chair conformation. The hydroxy and carbonyl O atoms face each other and are orientated to allow for the formation of the two intramolecular O—H⋯O hydrogen bonds which are typical of xanthene derivatives. In the...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201272/ https://www.ncbi.nlm.nih.gov/pubmed/22065620 http://dx.doi.org/10.1107/S1600536811038207 |
_version_ | 1782214836599390208 |
---|---|
author | Cha, Joo Hwan Son, Myung Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun |
author_facet | Cha, Joo Hwan Son, Myung Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun |
author_sort | Cha, Joo Hwan |
collection | PubMed |
description | In the title compound, C(22)H(24)O(5), each of the cyclohexenone rings adopts a half-chair conformation. The hydroxy and carbonyl O atoms face each other and are orientated to allow for the formation of the two intramolecular O—H⋯O hydrogen bonds which are typical of xanthene derivatives. In the crystal, weak intermolecular C—H⋯O hydrogen bonds link molecules into layers parallel to the ab plane. |
format | Online Article Text |
id | pubmed-3201272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32012722011-11-06 3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one Cha, Joo Hwan Son, Myung Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(22)H(24)O(5), each of the cyclohexenone rings adopts a half-chair conformation. The hydroxy and carbonyl O atoms face each other and are orientated to allow for the formation of the two intramolecular O—H⋯O hydrogen bonds which are typical of xanthene derivatives. In the crystal, weak intermolecular C—H⋯O hydrogen bonds link molecules into layers parallel to the ab plane. International Union of Crystallography 2011-09-30 /pmc/articles/PMC3201272/ /pubmed/22065620 http://dx.doi.org/10.1107/S1600536811038207 Text en © Cha 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 Cha, Joo Hwan Son, Myung Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun 3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one |
title | 3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one |
title_full | 3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one |
title_fullStr | 3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one |
title_full_unstemmed | 3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one |
title_short | 3-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one |
title_sort | 3-hydroxy-2-[(2e)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201272/ https://www.ncbi.nlm.nih.gov/pubmed/22065620 http://dx.doi.org/10.1107/S1600536811038207 |
work_keys_str_mv | AT chajoohwan 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT sonmyunghee 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT minsunjoon 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT choyongseo 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT leejaekyun 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one |