Cargando…
Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate
In the title compound, C(27)H(25)NO(4), the tetrahydropyridine ring adopts a half-chair conformation. The three phenyl rings form dihedral angles of 66.33 (7), 87.36 (8) and 36.90 (7)° with the least-squares plane through the tetrahydropyridine ring. The molecular conformation is stabilized by...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052159/ https://www.ncbi.nlm.nih.gov/pubmed/21522308 http://dx.doi.org/10.1107/S1600536811003266 |
_version_ | 1782199641473810432 |
---|---|
author | Aridoss, G. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. |
author_facet | Aridoss, G. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. |
author_sort | Aridoss, G. |
collection | PubMed |
description | In the title compound, C(27)H(25)NO(4), the tetrahydropyridine ring adopts a half-chair conformation. The three phenyl rings form dihedral angles of 66.33 (7), 87.36 (8) and 36.90 (7)° with the least-squares plane through the tetrahydropyridine ring. The molecular conformation is stabilized by an intramolecular O—H⋯O hydrogen bond, generating an S(6) motif. |
format | Text |
id | pubmed-3052159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30521592011-04-26 Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate Aridoss, G. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(25)NO(4), the tetrahydropyridine ring adopts a half-chair conformation. The three phenyl rings form dihedral angles of 66.33 (7), 87.36 (8) and 36.90 (7)° with the least-squares plane through the tetrahydropyridine ring. The molecular conformation is stabilized by an intramolecular O—H⋯O hydrogen bond, generating an S(6) motif. International Union of Crystallography 2011-02-02 /pmc/articles/PMC3052159/ /pubmed/21522308 http://dx.doi.org/10.1107/S1600536811003266 Text en © Aridoss et al. 2011 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 Aridoss, G. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate |
title | Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate |
title_full | Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate |
title_fullStr | Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate |
title_full_unstemmed | Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate |
title_short | Ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate |
title_sort | ethyl 1-benzoyl-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydropyridine-3-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052159/ https://www.ncbi.nlm.nih.gov/pubmed/21522308 http://dx.doi.org/10.1107/S1600536811003266 |
work_keys_str_mv | AT aridossg ethyl1benzoyl4hydroxy26diphenyl1256tetrahydropyridine3carboxylate AT sundaramoorthys ethyl1benzoyl4hydroxy26diphenyl1256tetrahydropyridine3carboxylate AT velmurugand ethyl1benzoyl4hydroxy26diphenyl1256tetrahydropyridine3carboxylate AT jeongyt ethyl1benzoyl4hydroxy26diphenyl1256tetrahydropyridine3carboxylate |