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2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid
In the title compound, C(30)H(46)O(3), an isolation product of Pistacia integerima Stewart, the five-membered ring is nearly in the envelope form. A 6-carboxyhept-5-en-2-yl group is attached to the five-membered ring. An S(6) ring motif is formed due to intramolecular C—H⋯O hydrogen bonding. In t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052128/ https://www.ncbi.nlm.nih.gov/pubmed/21522454 http://dx.doi.org/10.1107/S1600536811006283 |
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author | Arfan, Mohammad Rauf, Abdur Tahir, M. Nawaz Ali, Mumtaz Uddin, Ghias |
author_facet | Arfan, Mohammad Rauf, Abdur Tahir, M. Nawaz Ali, Mumtaz Uddin, Ghias |
author_sort | Arfan, Mohammad |
collection | PubMed |
description | In the title compound, C(30)H(46)O(3), an isolation product of Pistacia integerima Stewart, the five-membered ring is nearly in the envelope form. A 6-carboxyhept-5-en-2-yl group is attached to the five-membered ring. An S(6) ring motif is formed due to intramolecular C—H⋯O hydrogen bonding. In the crystal, intermolecular O—H⋯O hydrogen bonds form carboxylate dimers with R (2) (2)(8) ring motifs. |
format | Text |
id | pubmed-3052128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30521282011-04-26 2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid Arfan, Mohammad Rauf, Abdur Tahir, M. Nawaz Ali, Mumtaz Uddin, Ghias Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(30)H(46)O(3), an isolation product of Pistacia integerima Stewart, the five-membered ring is nearly in the envelope form. A 6-carboxyhept-5-en-2-yl group is attached to the five-membered ring. An S(6) ring motif is formed due to intramolecular C—H⋯O hydrogen bonding. In the crystal, intermolecular O—H⋯O hydrogen bonds form carboxylate dimers with R (2) (2)(8) ring motifs. International Union of Crystallography 2011-02-26 /pmc/articles/PMC3052128/ /pubmed/21522454 http://dx.doi.org/10.1107/S1600536811006283 Text en © Arfan 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 Arfan, Mohammad Rauf, Abdur Tahir, M. Nawaz Ali, Mumtaz Uddin, Ghias 2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid |
title | 2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid |
title_full | 2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid |
title_fullStr | 2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid |
title_full_unstemmed | 2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid |
title_short | 2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid |
title_sort | 2-methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052128/ https://www.ncbi.nlm.nih.gov/pubmed/21522454 http://dx.doi.org/10.1107/S1600536811006283 |
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