Cargando…
1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one
The title compound, C(26)H(34)O(9), a natural ent-kaurane diterpenoid, is composed of four rings with the expected cis and trans junctions. In the crystal structure, the molecules stack along the a axis and are linked together by intermolecular O—H⋯O hydrogen bonds.
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971301/ https://www.ncbi.nlm.nih.gov/pubmed/21578364 http://dx.doi.org/10.1107/S1600536809041828 |
_version_ | 1782190594536243200 |
---|---|
author | Yan, Fu-Lin Di, Xue-Mei Feng, Chuang Hou, Rei-Jie |
author_facet | Yan, Fu-Lin Di, Xue-Mei Feng, Chuang Hou, Rei-Jie |
author_sort | Yan, Fu-Lin |
collection | PubMed |
description | The title compound, C(26)H(34)O(9), a natural ent-kaurane diterpenoid, is composed of four rings with the expected cis and trans junctions. In the crystal structure, the molecules stack along the a axis and are linked together by intermolecular O—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-2971301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29713012010-12-30 1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one Yan, Fu-Lin Di, Xue-Mei Feng, Chuang Hou, Rei-Jie Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(26)H(34)O(9), a natural ent-kaurane diterpenoid, is composed of four rings with the expected cis and trans junctions. In the crystal structure, the molecules stack along the a axis and are linked together by intermolecular O—H⋯O hydrogen bonds. International Union of Crystallography 2009-10-17 /pmc/articles/PMC2971301/ /pubmed/21578364 http://dx.doi.org/10.1107/S1600536809041828 Text en © Yan et al. 2009 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 Yan, Fu-Lin Di, Xue-Mei Feng, Chuang Hou, Rei-Jie 1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one |
title | 1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one |
title_full | 1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one |
title_fullStr | 1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one |
title_full_unstemmed | 1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one |
title_short | 1α,11α,15β-Triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one |
title_sort | 1α,11α,15β-triacetoxy-7β-hydroxy-7α,20-epoxy-ent-kaur-16-en-6-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971301/ https://www.ncbi.nlm.nih.gov/pubmed/21578364 http://dx.doi.org/10.1107/S1600536809041828 |
work_keys_str_mv | AT yanfulin 1a11a15btriacetoxy7bhydroxy7a20epoxyentkaur16en6one AT dixuemei 1a11a15btriacetoxy7bhydroxy7a20epoxyentkaur16en6one AT fengchuang 1a11a15btriacetoxy7bhydroxy7a20epoxyentkaur16en6one AT houreijie 1a11a15btriacetoxy7bhydroxy7a20epoxyentkaur16en6one |