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Ethoxy­carbonyl­methyl ursolate

The title compound, C(34)H(54)O(5), was synthesized by the reaction of ursolic acid with ethyl chloro­acetate in the presence of DMA. All six-membered rings of the penta­cyclic triterpene skeleton adopt chair conformations. In the crystal structure, mol­ecules are linked by inter­molecular O—H⋯O hyd...

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Detalles Bibliográficos
Autores principales: Yang, Wei, Luo, Hua-ling, Yang, Cong-ling, Yin, Shu-fan, Li, Ying
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960021/
https://www.ncbi.nlm.nih.gov/pubmed/21581459
http://dx.doi.org/10.1107/S1600536808039706
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author Yang, Wei
Luo, Hua-ling
Yang, Cong-ling
Yin, Shu-fan
Li, Ying
author_facet Yang, Wei
Luo, Hua-ling
Yang, Cong-ling
Yin, Shu-fan
Li, Ying
author_sort Yang, Wei
collection PubMed
description The title compound, C(34)H(54)O(5), was synthesized by the reaction of ursolic acid with ethyl chloro­acetate in the presence of DMA. All six-membered rings of the penta­cyclic triterpene skeleton adopt chair conformations. In the crystal structure, mol­ecules are linked by inter­molecular O—H⋯O hydrogen-bond inter­actions, forming zigzag chains along the c axis.
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spelling pubmed-29600212010-12-30 Ethoxy­carbonyl­methyl ursolate Yang, Wei Luo, Hua-ling Yang, Cong-ling Yin, Shu-fan Li, Ying Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(34)H(54)O(5), was synthesized by the reaction of ursolic acid with ethyl chloro­acetate in the presence of DMA. All six-membered rings of the penta­cyclic triterpene skeleton adopt chair conformations. In the crystal structure, mol­ecules are linked by inter­molecular O—H⋯O hydrogen-bond inter­actions, forming zigzag chains along the c axis. International Union of Crystallography 2008-11-29 /pmc/articles/PMC2960021/ /pubmed/21581459 http://dx.doi.org/10.1107/S1600536808039706 Text en © Yang et al. 2008 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
Yang, Wei
Luo, Hua-ling
Yang, Cong-ling
Yin, Shu-fan
Li, Ying
Ethoxy­carbonyl­methyl ursolate
title Ethoxy­carbonyl­methyl ursolate
title_full Ethoxy­carbonyl­methyl ursolate
title_fullStr Ethoxy­carbonyl­methyl ursolate
title_full_unstemmed Ethoxy­carbonyl­methyl ursolate
title_short Ethoxy­carbonyl­methyl ursolate
title_sort ethoxy­carbonyl­methyl ursolate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960021/
https://www.ncbi.nlm.nih.gov/pubmed/21581459
http://dx.doi.org/10.1107/S1600536808039706
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AT yangcongling ethoxycarbonylmethylursolate
AT yinshufan ethoxycarbonylmethylursolate
AT liying ethoxycarbonylmethylursolate