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19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone
The title compound, C(27)H(34)O(5), a beyerane-type diterpenoid prepared by peroxidation and benzoylation of isosteviol, contains a fused six-membered ring system. The O atoms of the benzoic ester and the lactone are disordered with occupancy ratios of 0.6 (4):0.4 (4) and 0.6 (2):0.4 (2), respectiv...
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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/PMC3050127/ https://www.ncbi.nlm.nih.gov/pubmed/21522644 http://dx.doi.org/10.1107/S1600536810051561 |
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author | Cai, Jin Zha, Xiaoming |
author_facet | Cai, Jin Zha, Xiaoming |
author_sort | Cai, Jin |
collection | PubMed |
description | The title compound, C(27)H(34)O(5), a beyerane-type diterpenoid prepared by peroxidation and benzoylation of isosteviol, contains a fused six-membered ring system. The O atoms of the benzoic ester and the lactone are disordered with occupancy ratios of 0.6 (4):0.4 (4) and 0.6 (2):0.4 (2), respectively. Three cyclohexane rings have chair conformations, whereas the remaining lactone ring adopts a half-chair conformation. |
format | Text |
id | pubmed-3050127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30501272011-04-26 19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone Cai, Jin Zha, Xiaoming Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(27)H(34)O(5), a beyerane-type diterpenoid prepared by peroxidation and benzoylation of isosteviol, contains a fused six-membered ring system. The O atoms of the benzoic ester and the lactone are disordered with occupancy ratios of 0.6 (4):0.4 (4) and 0.6 (2):0.4 (2), respectively. Three cyclohexane rings have chair conformations, whereas the remaining lactone ring adopts a half-chair conformation. International Union of Crystallography 2010-12-15 /pmc/articles/PMC3050127/ /pubmed/21522644 http://dx.doi.org/10.1107/S1600536810051561 Text en © Cai and Zha 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 Cai, Jin Zha, Xiaoming 19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone |
title | 19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone |
title_full | 19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone |
title_fullStr | 19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone |
title_full_unstemmed | 19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone |
title_short | 19-Benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone |
title_sort | 19-benzoyloxy-13,16-seco-ent-beyeran 13,16-lactone |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050127/ https://www.ncbi.nlm.nih.gov/pubmed/21522644 http://dx.doi.org/10.1107/S1600536810051561 |
work_keys_str_mv | AT caijin 19benzoyloxy1316secoentbeyeran1316lactone AT zhaxiaoming 19benzoyloxy1316secoentbeyeran1316lactone |