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1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one
In the title cycloadduct, C(20)H(18)N(4)O(5), the rings of the pyrrolizine system adopt envelope conformations. A centrosymmetric dimer is formed via intermolecular N—H⋯O hydrogen bonds between the indolinone rings.
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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/PMC2960711/ https://www.ncbi.nlm.nih.gov/pubmed/21201723 http://dx.doi.org/10.1107/S1600536808025038 |
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author | Sarrafi, Yaghoub Alimohammadi, Kamal |
author_facet | Sarrafi, Yaghoub Alimohammadi, Kamal |
author_sort | Sarrafi, Yaghoub |
collection | PubMed |
description | In the title cycloadduct, C(20)H(18)N(4)O(5), the rings of the pyrrolizine system adopt envelope conformations. A centrosymmetric dimer is formed via intermolecular N—H⋯O hydrogen bonds between the indolinone rings. |
format | Text |
id | pubmed-2960711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29607112010-12-30 1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one Sarrafi, Yaghoub Alimohammadi, Kamal Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title cycloadduct, C(20)H(18)N(4)O(5), the rings of the pyrrolizine system adopt envelope conformations. A centrosymmetric dimer is formed via intermolecular N—H⋯O hydrogen bonds between the indolinone rings. International Union of Crystallography 2008-08-13 /pmc/articles/PMC2960711/ /pubmed/21201723 http://dx.doi.org/10.1107/S1600536808025038 Text en © Sarrafi and Alimohammadi 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 Sarrafi, Yaghoub Alimohammadi, Kamal 1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one |
title | 1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one |
title_full | 1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one |
title_fullStr | 1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one |
title_full_unstemmed | 1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one |
title_short | 1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one |
title_sort | 1′,5-dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a’-hexahydrospiro[indoline-3,3′-1′h-pyrrolizin]-2-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960711/ https://www.ncbi.nlm.nih.gov/pubmed/21201723 http://dx.doi.org/10.1107/S1600536808025038 |
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