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(4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound
The new title diterpenoid compound, C(20)H(30)O, is a natural product isolated from Tetraclinis articulata wood via chloroform extraction. The asymmetric unit contains four molecules with the same S,S configuration, deduced from the chemical synthesis. Indeed, an overlay analysis, calculated usin...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960765/ https://www.ncbi.nlm.nih.gov/pubmed/21201941 http://dx.doi.org/10.1107/S1600536808004546 |
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author | Zeroual, Abdellah Mazoir, Noureddine Daran, Jean-Claude Akssira, Mohamed Benharref, Ahmed |
author_facet | Zeroual, Abdellah Mazoir, Noureddine Daran, Jean-Claude Akssira, Mohamed Benharref, Ahmed |
author_sort | Zeroual, Abdellah |
collection | PubMed |
description | The new title diterpenoid compound, C(20)H(30)O, is a natural product isolated from Tetraclinis articulata wood via chloroform extraction. The asymmetric unit contains four molecules with the same S,S configuration, deduced from the chemical synthesis. Indeed, an overlay analysis, calculated using structure-matching software, shows that the four molecules can be superimposed. The central ring has a half-chair conformation, whereas the saturated ring displays a chair conformation. |
format | Text |
id | pubmed-2960765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29607652010-12-30 (4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound Zeroual, Abdellah Mazoir, Noureddine Daran, Jean-Claude Akssira, Mohamed Benharref, Ahmed Acta Crystallogr Sect E Struct Rep Online Organic Papers The new title diterpenoid compound, C(20)H(30)O, is a natural product isolated from Tetraclinis articulata wood via chloroform extraction. The asymmetric unit contains four molecules with the same S,S configuration, deduced from the chemical synthesis. Indeed, an overlay analysis, calculated using structure-matching software, shows that the four molecules can be superimposed. The central ring has a half-chair conformation, whereas the saturated ring displays a chair conformation. International Union of Crystallography 2008-02-20 /pmc/articles/PMC2960765/ /pubmed/21201941 http://dx.doi.org/10.1107/S1600536808004546 Text en © Zeroual et al. 2008 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 Zeroual, Abdellah Mazoir, Noureddine Daran, Jean-Claude Akssira, Mohamed Benharref, Ahmed (4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound |
title | (4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound |
title_full | (4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound |
title_fullStr | (4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound |
title_full_unstemmed | (4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound |
title_short | (4aS,10aS)-7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound |
title_sort | (4as,10as)-7-hydroxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene: a new diterpenoid compound |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960765/ https://www.ncbi.nlm.nih.gov/pubmed/21201941 http://dx.doi.org/10.1107/S1600536808004546 |
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