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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...

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Detalles Bibliográficos
Autores principales: Bibila Mayaya Bisseyou, Yvon, Timotou, Adéyolé, Adjou, Ajouby, Kakou-Yao, Rita, Tenon Abodou, Jules
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
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.
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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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