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Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate
In the title compound, C(16)H(17)N(3)O(4), the six-membered N-containing ring adopts a half-chair conformation. One C atom of the five-membered ring is disordered over two sites, with occupancy factors of ca 0.67 and 0.33. The major pyrroline component adopts a half-chair conformation. Intermolecul...
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/PMC3275286/ https://www.ncbi.nlm.nih.gov/pubmed/22347142 http://dx.doi.org/10.1107/S1600536812003480 |
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author | Bibila Mayaya Bisseyou, Yvon Timotou, Adéyolé Adjou, Ajouby Kakou-Yao, Rita Tenon Abodou, Jules |
author_facet | Bibila Mayaya Bisseyou, Yvon Timotou, Adéyolé Adjou, Ajouby Kakou-Yao, Rita Tenon Abodou, Jules |
author_sort | Bibila Mayaya Bisseyou, Yvon |
collection | PubMed |
description | In the title compound, C(16)H(17)N(3)O(4), the six-membered N-containing ring adopts a half-chair conformation. One C atom of the five-membered ring is disordered over two sites, with occupancy factors of ca 0.67 and 0.33. The major pyrroline component adopts a half-chair conformation. Intermolecular C—H⋯O hydrogen bonds forming centrosymmetric dimers are observed in the crystal. |
format | Online Article Text |
id | pubmed-3275286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32752862012-02-15 Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate Bibila Mayaya Bisseyou, Yvon Timotou, Adéyolé Adjou, Ajouby Kakou-Yao, Rita Tenon Abodou, Jules Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(17)N(3)O(4), the six-membered N-containing ring adopts a half-chair conformation. One C atom of the five-membered ring is disordered over two sites, with occupancy factors of ca 0.67 and 0.33. The major pyrroline component adopts a half-chair conformation. Intermolecular C—H⋯O hydrogen bonds forming centrosymmetric dimers are observed in the crystal. International Union of Crystallography 2012-01-31 /pmc/articles/PMC3275286/ /pubmed/22347142 http://dx.doi.org/10.1107/S1600536812003480 Text en © Bibila Mayaya Bisseyou 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 Bibila Mayaya Bisseyou, Yvon Timotou, Adéyolé Adjou, Ajouby Kakou-Yao, Rita Tenon Abodou, Jules Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate |
title | Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate |
title_full | Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate |
title_fullStr | Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate |
title_full_unstemmed | Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate |
title_short | Ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate |
title_sort | ethyl 4-cyano-7-nitro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoline-4-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275286/ https://www.ncbi.nlm.nih.gov/pubmed/22347142 http://dx.doi.org/10.1107/S1600536812003480 |
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