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rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate
The racemic title compound, C(22)H(23)BrO(4)S, crystallizes with two molecules in the asymmetric unit. The dihedral angles between the thiophene and phenyl rings are 71.64 (17) and 73.41 (17)°.
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959655/ https://www.ncbi.nlm.nih.gov/pubmed/21581012 http://dx.doi.org/10.1107/S1600536808032650 |
| _version_ | 1782188551627079680 |
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| author | Fischer, Andreas Swamy, M. T. Narayana, B. Yathirajan, H. S. |
| author_facet | Fischer, Andreas Swamy, M. T. Narayana, B. Yathirajan, H. S. |
| author_sort | Fischer, Andreas |
| collection | PubMed |
| description | The racemic title compound, C(22)H(23)BrO(4)S, crystallizes with two molecules in the asymmetric unit. The dihedral angles between the thiophene and phenyl rings are 71.64 (17) and 73.41 (17)°. |
| format | Text |
| id | pubmed-2959655 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2008 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29596552010-12-30 rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate Fischer, Andreas Swamy, M. T. Narayana, B. Yathirajan, H. S. Acta Crystallogr Sect E Struct Rep Online Organic Papers The racemic title compound, C(22)H(23)BrO(4)S, crystallizes with two molecules in the asymmetric unit. The dihedral angles between the thiophene and phenyl rings are 71.64 (17) and 73.41 (17)°. International Union of Crystallography 2008-10-22 /pmc/articles/PMC2959655/ /pubmed/21581012 http://dx.doi.org/10.1107/S1600536808032650 Text en © Fischer 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 Fischer, Andreas Swamy, M. T. Narayana, B. Yathirajan, H. S. rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate |
| title |
rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate |
| title_full |
rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate |
| title_fullStr |
rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate |
| title_full_unstemmed |
rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate |
| title_short |
rac-Ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate |
| title_sort | rac-ethyl 3-(3-bromo-2-thienyl)-2-oxo-6-(4-propoxyphenyl)cyclohex-3-ene-1-carboxylate |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959655/ https://www.ncbi.nlm.nih.gov/pubmed/21581012 http://dx.doi.org/10.1107/S1600536808032650 |
| work_keys_str_mv | AT fischerandreas racethyl33bromo2thienyl2oxo64propoxyphenylcyclohex3ene1carboxylate AT swamymt racethyl33bromo2thienyl2oxo64propoxyphenylcyclohex3ene1carboxylate AT narayanab racethyl33bromo2thienyl2oxo64propoxyphenylcyclohex3ene1carboxylate AT yathirajanhs racethyl33bromo2thienyl2oxo64propoxyphenylcyclohex3ene1carboxylate |