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, C22H24O5, 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&#8212;H...O hydrogen bonds which are typical of xanthene derivatives....

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Main Authors:	Jae Kyun Lee, Yong Seo Cho, Sun-Joon Min, Myung Hee Son, Joo Hwan Cha
Format:	Article
Language:	English
Published:	International Union of Crystallography 2011-10-01
Series:	Acta Crystallographica Section E
Online Access:	http://scripts.iucr.org/cgi-bin/paper?S1600536811038207

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record_format	Article
spelling	doaj-b2ae6ef653c545498b0901e810f5b5b22020-11-25T01:09:42ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682011-10-016710o2739o273910.1107/S16005368110382073-Hydroxy-2-[(2E)-1-(2-hydroxy-6-oxocyclohex-1-en-1-yl)-3-(2-methoxyphenyl)prop-2-en-1-yl]cyclohex-2-en-1-oneJae Kyun LeeYong Seo ChoSun-Joon MinMyung Hee SonJoo Hwan ChaIn the title compound, C22H24O5, 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&#8212;H...O hydrogen bonds which are typical of xanthene derivatives. In the crystal, weak intermolecular C&#8212;H...O hydrogen bonds link molecules into layers parallel to the ab plane.http://scripts.iucr.org/cgi-bin/paper?S1600536811038207
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Jae Kyun Lee Yong Seo Cho Sun-Joon Min Myung Hee Son Joo Hwan Cha
spellingShingle	Jae Kyun Lee Yong Seo Cho Sun-Joon Min Myung Hee Son Joo Hwan Cha 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 Acta Crystallographica Section E
author_facet	Jae Kyun Lee Yong Seo Cho Sun-Joon Min Myung Hee Son Joo Hwan Cha
author_sort	Jae Kyun Lee
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_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_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_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
publisher	International Union of Crystallography
series	Acta Crystallographica Section E
issn	1600-5368
publishDate	2011-10-01
description	In the title compound, C22H24O5, 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&#8212;H...O hydrogen bonds which are typical of xanthene derivatives. In the crystal, weak intermolecular C&#8212;H...O hydrogen bonds link molecules into layers parallel to the ab plane.
url	http://scripts.iucr.org/cgi-bin/paper?S1600536811038207
work_keys_str_mv	AT jaekyunlee 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT yongseocho 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT sunjoonmin 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT myungheeson 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one AT joohwancha 3hydroxy22e12hydroxy6oxocyclohex1en1yl32methoxyphenylprop2en1ylcyclohex2en1one
_version_	1725177124694786048

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

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