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6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene

The title compound, C(24)H(34)O(8), a natural ent-kaurane diterpenoid, is composed of four rings with the expected cis and trans junctions. The crystal structure is stabilized by inter­molecular O—H⋯O hydrogen bonds. In addition, an intra­molecular O—H⋯O hydrogen bond occurs.

Detalles Bibliográficos
Autores principales: Di, Xue-Mei, Yan, Fu-Lin, Feng, Chuang, Cui, Jian-Min
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979703/
https://www.ncbi.nlm.nih.gov/pubmed/21579784
http://dx.doi.org/10.1107/S1600536810001170
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author Di, Xue-Mei
Yan, Fu-Lin
Feng, Chuang
Cui, Jian-Min
author_facet Di, Xue-Mei
Yan, Fu-Lin
Feng, Chuang
Cui, Jian-Min
author_sort Di, Xue-Mei
collection PubMed
description The title compound, C(24)H(34)O(8), a natural ent-kaurane diterpenoid, is composed of four rings with the expected cis and trans junctions. The crystal structure is stabilized by inter­molecular O—H⋯O hydrogen bonds. In addition, an intra­molecular O—H⋯O hydrogen bond occurs.
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spelling pubmed-29797032010-12-30 6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene Di, Xue-Mei Yan, Fu-Lin Feng, Chuang Cui, Jian-Min Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(34)O(8), a natural ent-kaurane diterpenoid, is composed of four rings with the expected cis and trans junctions. The crystal structure is stabilized by inter­molecular O—H⋯O hydrogen bonds. In addition, an intra­molecular O—H⋯O hydrogen bond occurs. International Union of Crystallography 2010-01-16 /pmc/articles/PMC2979703/ /pubmed/21579784 http://dx.doi.org/10.1107/S1600536810001170 Text en © Di et al. 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
Di, Xue-Mei
Yan, Fu-Lin
Feng, Chuang
Cui, Jian-Min
6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene
title 6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene
title_full 6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene
title_fullStr 6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene
title_full_unstemmed 6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene
title_short 6β,15β-Diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene
title_sort 6β,15β-diacet­oxy-1β,7β,13α-trihydr­oxy-7α,20-ep­oxy-ent-kaur-16-ene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979703/
https://www.ncbi.nlm.nih.gov/pubmed/21579784
http://dx.doi.org/10.1107/S1600536810001170
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