Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Junqing, Zha, Xiaoming
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
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
_version_ 1782191893110587392
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