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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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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. |
format | Text |
id | pubmed-2960021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT yangwei ethoxycarbonylmethylursolate AT luohualing ethoxycarbonylmethylursolate AT yangcongling ethoxycarbonylmethylursolate AT yinshufan ethoxycarbonylmethylursolate AT liying ethoxycarbonylmethylursolate |