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c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide
In the title compound, C(26)H(26)N(2)O(2), the piperidinone ring adopts a distorted boat conformation. The two phenyl rings substituted at positions 2 and 6 of the piperidinone ring occupy axial and equatorial orientations, which are approximately perpendicular to each other [89.14 (8)°]. The phenyl...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971303/ https://www.ncbi.nlm.nih.gov/pubmed/21578400 http://dx.doi.org/10.1107/S1600536809041579 |
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author | Thenmozhi, M. Kavitha, T. Ponnuswamy, S. Jamesh, M. Ponnuswamy, M. N. |
author_facet | Thenmozhi, M. Kavitha, T. Ponnuswamy, S. Jamesh, M. Ponnuswamy, M. N. |
author_sort | Thenmozhi, M. |
collection | PubMed |
description | In the title compound, C(26)H(26)N(2)O(2), the piperidinone ring adopts a distorted boat conformation. The two phenyl rings substituted at positions 2 and 6 of the piperidinone ring occupy axial and equatorial orientations, which are approximately perpendicular to each other [89.14 (8)°]. The phenylcarbamoyl group adopts an extended conformation. The crystal structure is stabilized by intermolecular C—H⋯O interactions. |
format | Text |
id | pubmed-2971303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29713032010-12-30 c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide Thenmozhi, M. Kavitha, T. Ponnuswamy, S. Jamesh, M. Ponnuswamy, M. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(26)H(26)N(2)O(2), the piperidinone ring adopts a distorted boat conformation. The two phenyl rings substituted at positions 2 and 6 of the piperidinone ring occupy axial and equatorial orientations, which are approximately perpendicular to each other [89.14 (8)°]. The phenylcarbamoyl group adopts an extended conformation. The crystal structure is stabilized by intermolecular C—H⋯O interactions. International Union of Crystallography 2009-10-23 /pmc/articles/PMC2971303/ /pubmed/21578400 http://dx.doi.org/10.1107/S1600536809041579 Text en © Thenmozhi et al. 2009 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 Thenmozhi, M. Kavitha, T. Ponnuswamy, S. Jamesh, M. Ponnuswamy, M. N. c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide |
title |
c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide |
title_full |
c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide |
title_fullStr |
c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide |
title_full_unstemmed |
c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide |
title_short |
c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide |
title_sort | c-3,t-3-dimethyl-4-oxo-r-2,c-6-diphenylpiperidine-1-carboxamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971303/ https://www.ncbi.nlm.nih.gov/pubmed/21578400 http://dx.doi.org/10.1107/S1600536809041579 |
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