Cargando…

6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide

The title eremophilenolide, C(15)H(22)O(3), is a natural compound isolated from Senecio laetus Edgew. The two cis-fused six-membered rings have chair confomations and the five-membered ring has a planar envelope conformation [maximum deviation = 0.010 (1) Å]. The β-hy­droxy group participates in int...

Descripción completa

Detalles Bibliográficos
Autores principales: Su, Ri-Na, Shi, Sha, Wu, Hai-Bo, Wang, Wen-Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120521/
https://www.ncbi.nlm.nih.gov/pubmed/21754755
http://dx.doi.org/10.1107/S1600536811016308
_version_ 1782206697962471424
author Su, Ri-Na
Shi, Sha
Wu, Hai-Bo
Wang, Wen-Shu
author_facet Su, Ri-Na
Shi, Sha
Wu, Hai-Bo
Wang, Wen-Shu
author_sort Su, Ri-Na
collection PubMed
description The title eremophilenolide, C(15)H(22)O(3), is a natural compound isolated from Senecio laetus Edgew. The two cis-fused six-membered rings have chair confomations and the five-membered ring has a planar envelope conformation [maximum deviation = 0.010 (1) Å]. The β-hy­droxy group participates in inter­molecular O—H⋯O hydrogen bonding, forming mol­ecular chains along the a axis.
format Online
Article
Text
id pubmed-3120521
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-31205212011-07-13 6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide Su, Ri-Na Shi, Sha Wu, Hai-Bo Wang, Wen-Shu Acta Crystallogr Sect E Struct Rep Online Organic Papers The title eremophilenolide, C(15)H(22)O(3), is a natural compound isolated from Senecio laetus Edgew. The two cis-fused six-membered rings have chair confomations and the five-membered ring has a planar envelope conformation [maximum deviation = 0.010 (1) Å]. The β-hy­droxy group participates in inter­molecular O—H⋯O hydrogen bonding, forming mol­ecular chains along the a axis. International Union of Crystallography 2011-05-07 /pmc/articles/PMC3120521/ /pubmed/21754755 http://dx.doi.org/10.1107/S1600536811016308 Text en © Su 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
Su, Ri-Na
Shi, Sha
Wu, Hai-Bo
Wang, Wen-Shu
6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide
title 6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide
title_full 6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide
title_fullStr 6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide
title_full_unstemmed 6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide
title_short 6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide
title_sort 6β-hy­droxy­eremophil-7(11)-en-8β,12-olide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120521/
https://www.ncbi.nlm.nih.gov/pubmed/21754755
http://dx.doi.org/10.1107/S1600536811016308
work_keys_str_mv AT surina 6bhydroxyeremophil711en8b12olide
AT shisha 6bhydroxyeremophil711en8b12olide
AT wuhaibo 6bhydroxyeremophil711en8b12olide
AT wangwenshu 6bhydroxyeremophil711en8b12olide