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4′-Bromobutyl ent-16-oxobeyeran-19-oate
The title compound, C(24)H(37)BrO(3), is a tetracyclic diterpenoid with a beyerane skeleton, synthesized by esterification of isosteviol. It comprises a fused four-ring system A/B/C/D. Rings A and B have a chair conformation, whereas ring C is an unsymmetrical distorted chair; the remaining five-me...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983525/ https://www.ncbi.nlm.nih.gov/pubmed/21580366 http://dx.doi.org/10.1107/S1600536810005167 |
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author | Chen, Junqing Zha, Xiaoming |
author_facet | Chen, Junqing Zha, Xiaoming |
author_sort | Chen, Junqing |
collection | PubMed |
description | The title compound, C(24)H(37)BrO(3), is a tetracyclic diterpenoid with a beyerane skeleton, synthesized by esterification of isosteviol. It comprises a fused four-ring system A/B/C/D. Rings A and B have a chair conformation, whereas ring C is an unsymmetrical distorted chair; the remaining five-membered ring D adopts an envelope conformation. The stereochemistry of the A/B and B/C ring junctions are trans, while the C/D junction is cis. |
format | Text |
id | pubmed-2983525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29835252010-12-30 4′-Bromobutyl ent-16-oxobeyeran-19-oate Chen, Junqing Zha, Xiaoming Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(37)BrO(3), is a tetracyclic diterpenoid with a beyerane skeleton, synthesized by esterification of isosteviol. It comprises a fused four-ring system A/B/C/D. Rings A and B have a chair conformation, whereas ring C is an unsymmetrical distorted chair; the remaining five-membered ring D adopts an envelope conformation. The stereochemistry of the A/B and B/C ring junctions are trans, while the C/D junction is cis. International Union of Crystallography 2010-02-13 /pmc/articles/PMC2983525/ /pubmed/21580366 http://dx.doi.org/10.1107/S1600536810005167 Text en © Chen and Zha 2010 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 Chen, Junqing Zha, Xiaoming 4′-Bromobutyl ent-16-oxobeyeran-19-oate |
title | 4′-Bromobutyl ent-16-oxobeyeran-19-oate |
title_full | 4′-Bromobutyl ent-16-oxobeyeran-19-oate |
title_fullStr | 4′-Bromobutyl ent-16-oxobeyeran-19-oate |
title_full_unstemmed | 4′-Bromobutyl ent-16-oxobeyeran-19-oate |
title_short | 4′-Bromobutyl ent-16-oxobeyeran-19-oate |
title_sort | 4′-bromobutyl ent-16-oxobeyeran-19-oate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983525/ https://www.ncbi.nlm.nih.gov/pubmed/21580366 http://dx.doi.org/10.1107/S1600536810005167 |
work_keys_str_mv | AT chenjunqing 4bromobutylent16oxobeyeran19oate AT zhaxiaoming 4bromobutylent16oxobeyeran19oate |