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Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)

In the title compound, C(15)H(22)O(3), the five-membered ring displays an envelope conformation, whereas the two six-membered rings show different conformations, viz. chair and half-chair. In the crystal, mol­ecules are linked through inter­molecular O—H⋯O hydrogen bonds, forming chains running alon...

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Detalles Bibliográficos
Autores principales: Cheng, Jing-Li, Zhou, Yong, Lin, Fu-Cheng, Zhao, Jin-Hao, Zhu, Guo-Nian
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971347/
https://www.ncbi.nlm.nih.gov/pubmed/21578465
http://dx.doi.org/10.1107/S1600536809044080
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author Cheng, Jing-Li
Zhou, Yong
Lin, Fu-Cheng
Zhao, Jin-Hao
Zhu, Guo-Nian
author_facet Cheng, Jing-Li
Zhou, Yong
Lin, Fu-Cheng
Zhao, Jin-Hao
Zhu, Guo-Nian
author_sort Cheng, Jing-Li
collection PubMed
description In the title compound, C(15)H(22)O(3), the five-membered ring displays an envelope conformation, whereas the two six-membered rings show different conformations, viz. chair and half-chair. In the crystal, mol­ecules are linked through inter­molecular O—H⋯O hydrogen bonds, forming chains running along the b axis.
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spelling pubmed-29713472010-12-30 Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene) Cheng, Jing-Li Zhou, Yong Lin, Fu-Cheng Zhao, Jin-Hao Zhu, Guo-Nian Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(22)O(3), the five-membered ring displays an envelope conformation, whereas the two six-membered rings show different conformations, viz. chair and half-chair. In the crystal, mol­ecules are linked through inter­molecular O—H⋯O hydrogen bonds, forming chains running along the b axis. International Union of Crystallography 2009-10-28 /pmc/articles/PMC2971347/ /pubmed/21578465 http://dx.doi.org/10.1107/S1600536809044080 Text en © Cheng et al. 2009 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
Cheng, Jing-Li
Zhou, Yong
Lin, Fu-Cheng
Zhao, Jin-Hao
Zhu, Guo-Nian
Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)
title Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)
title_full Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)
title_fullStr Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)
title_full_unstemmed Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)
title_short Trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)
title_sort trichodermol (4α-hydr­oxy-12,13-epoxy­trichothec-9-ene)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971347/
https://www.ncbi.nlm.nih.gov/pubmed/21578465
http://dx.doi.org/10.1107/S1600536809044080
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