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r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one
In the title compound, C(19)H(19)F(2)NO, the piperidinone ring adopts a chair conformation. The crystal packing is stabilized by C—H⋯O and C—H⋯F intermolecular interactions, generating centrosymmetric dimers of R (2) (2)(14) and R (2) (2)(24) rings.
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960264/ https://www.ncbi.nlm.nih.gov/pubmed/21201456 http://dx.doi.org/10.1107/S1600536807068699 |
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author | Gayathri, D. Velmurugan, D. Aridoss, G. Kabilan, S. Ravikumar, K. |
author_facet | Gayathri, D. Velmurugan, D. Aridoss, G. Kabilan, S. Ravikumar, K. |
author_sort | Gayathri, D. |
collection | PubMed |
description | In the title compound, C(19)H(19)F(2)NO, the piperidinone ring adopts a chair conformation. The crystal packing is stabilized by C—H⋯O and C—H⋯F intermolecular interactions, generating centrosymmetric dimers of R (2) (2)(14) and R (2) (2)(24) rings. |
format | Text |
id | pubmed-2960264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29602642010-12-30 r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one Gayathri, D. Velmurugan, D. Aridoss, G. Kabilan, S. Ravikumar, K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(19)F(2)NO, the piperidinone ring adopts a chair conformation. The crystal packing is stabilized by C—H⋯O and C—H⋯F intermolecular interactions, generating centrosymmetric dimers of R (2) (2)(14) and R (2) (2)(24) rings. International Union of Crystallography 2008-01-11 /pmc/articles/PMC2960264/ /pubmed/21201456 http://dx.doi.org/10.1107/S1600536807068699 Text en © Gayathri et al. 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 Gayathri, D. Velmurugan, D. Aridoss, G. Kabilan, S. Ravikumar, K. r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one |
title |
r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one |
title_full |
r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one |
title_fullStr |
r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one |
title_full_unstemmed |
r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one |
title_short |
r-2,c-6-Bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one |
title_sort | r-2,c-6-bis(4-fluorophenyl)-t-3,t-5-dimethylpiperidin-4-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960264/ https://www.ncbi.nlm.nih.gov/pubmed/21201456 http://dx.doi.org/10.1107/S1600536807068699 |
work_keys_str_mv | AT gayathrid r2c6bis4fluorophenylt3t5dimethylpiperidin4one AT velmurugand r2c6bis4fluorophenylt3t5dimethylpiperidin4one AT aridossg r2c6bis4fluorophenylt3t5dimethylpiperidin4one AT kabilans r2c6bis4fluorophenylt3t5dimethylpiperidin4one AT ravikumark r2c6bis4fluorophenylt3t5dimethylpiperidin4one |