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c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone
In the title compound, C(17)H(19)NO(8) [systematic name = dimethyl 4-hydroxy-4-methyl-2-(3-nitrophenyl)-6-oxocyclohexane-1,3-dicarboxylate], the cyclohexanone ring exhibits a chair conformation. The methoxycarbonyl groups are oriented in opposite directions with respect to the cyclohexanone ri...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394008/ https://www.ncbi.nlm.nih.gov/pubmed/22798873 http://dx.doi.org/10.1107/S1600536812027377 |
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author | Rizwana Begum, S. Hema, R. Pandiarajan, K. Balasubramanian, Sridhar Anitha, A.G. |
author_facet | Rizwana Begum, S. Hema, R. Pandiarajan, K. Balasubramanian, Sridhar Anitha, A.G. |
author_sort | Rizwana Begum, S. |
collection | PubMed |
description | In the title compound, C(17)H(19)NO(8) [systematic name = dimethyl 4-hydroxy-4-methyl-2-(3-nitrophenyl)-6-oxocyclohexane-1,3-dicarboxylate], the cyclohexanone ring exhibits a chair conformation. The methoxycarbonyl groups are oriented in opposite directions with respect to the cyclohexanone ring. In the crystal, O—H⋯O hydrogen bonds links the molecules into chains running parallel to the a axis. These chains are connected by weak C—H⋯O hydrogen bonds, forming sheets parallel to the ab plane. |
format | Online Article Text |
id | pubmed-3394008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33940082012-07-13 c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone Rizwana Begum, S. Hema, R. Pandiarajan, K. Balasubramanian, Sridhar Anitha, A.G. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(19)NO(8) [systematic name = dimethyl 4-hydroxy-4-methyl-2-(3-nitrophenyl)-6-oxocyclohexane-1,3-dicarboxylate], the cyclohexanone ring exhibits a chair conformation. The methoxycarbonyl groups are oriented in opposite directions with respect to the cyclohexanone ring. In the crystal, O—H⋯O hydrogen bonds links the molecules into chains running parallel to the a axis. These chains are connected by weak C—H⋯O hydrogen bonds, forming sheets parallel to the ab plane. International Union of Crystallography 2012-06-27 /pmc/articles/PMC3394008/ /pubmed/22798873 http://dx.doi.org/10.1107/S1600536812027377 Text en © Rizwana Begum et al. 2012 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 Rizwana Begum, S. Hema, R. Pandiarajan, K. Balasubramanian, Sridhar Anitha, A.G. c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone |
title |
c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone |
title_full |
c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone |
title_fullStr |
c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone |
title_full_unstemmed |
c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone |
title_short |
c-5-Hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone |
title_sort | c-5-hydroxy-r-2,c-4-bis(methoxycarbonyl)-t-5-methyl-t-3-(3-nitrophenyl)cyclohexanone |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394008/ https://www.ncbi.nlm.nih.gov/pubmed/22798873 http://dx.doi.org/10.1107/S1600536812027377 |
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