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(E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione

In the title compound, C(21)H(19)ClO(3), the two cyclo­hexenone rings adopt half-chair conformations, whereas the pyran ring adopts a boat conformation. The 4-chloro­phenyl ring is almost perpendicular to the plane through the four C atoms of the pyran ring [dihedral angle = 87.97 (6)°]. In the crys...

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Autores principales: Lee, Jae Kyun, Pae, Ae Nim, Cho, Yong Seo, Cha, Joo Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275246/
https://www.ncbi.nlm.nih.gov/pubmed/22347102
http://dx.doi.org/10.1107/S1600536812002139
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author Lee, Jae Kyun
Pae, Ae Nim
Cho, Yong Seo
Cha, Joo Hwan
author_facet Lee, Jae Kyun
Pae, Ae Nim
Cho, Yong Seo
Cha, Joo Hwan
author_sort Lee, Jae Kyun
collection PubMed
description In the title compound, C(21)H(19)ClO(3), the two cyclo­hexenone rings adopt half-chair conformations, whereas the pyran ring adopts a boat conformation. The 4-chloro­phenyl ring is almost perpendicular to the plane through the four C atoms of the pyran ring [dihedral angle = 87.97 (6)°]. In the crystal, weak C—H⋯O hydrogen bonds link the mol­ecules into a chain parallel to the a-axis.
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spelling pubmed-32752462012-02-15 (E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione Lee, Jae Kyun Pae, Ae Nim Cho, Yong Seo Cha, Joo Hwan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(19)ClO(3), the two cyclo­hexenone rings adopt half-chair conformations, whereas the pyran ring adopts a boat conformation. The 4-chloro­phenyl ring is almost perpendicular to the plane through the four C atoms of the pyran ring [dihedral angle = 87.97 (6)°]. In the crystal, weak C—H⋯O hydrogen bonds link the mol­ecules into a chain parallel to the a-axis. International Union of Crystallography 2012-01-21 /pmc/articles/PMC3275246/ /pubmed/22347102 http://dx.doi.org/10.1107/S1600536812002139 Text en © Lee 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
Lee, Jae Kyun
Pae, Ae Nim
Cho, Yong Seo
Cha, Joo Hwan
(E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione
title (E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione
title_full (E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione
title_fullStr (E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione
title_full_unstemmed (E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione
title_short (E)-9-(4-Chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2H-xanthene-1,8-dione
title_sort (e)-9-(4-chloro­styr­yl)-3,4,5,6,7,9-hexa­hydro-2h-xanthene-1,8-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275246/
https://www.ncbi.nlm.nih.gov/pubmed/22347102
http://dx.doi.org/10.1107/S1600536812002139
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