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Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline
In the title compound, C(16)H(17)NO(2)S, the heterocyclic ring adopts a half-chair conformation and the bond-angle sum at the N atom is 354.6°. The dihedral angle between the planes of the aromatic rings is 74.15 (10)°. In the crystal, molecules are linked by weak C—H⋯O hydrogen bonds, generating C...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438803/ https://www.ncbi.nlm.nih.gov/pubmed/26029439 http://dx.doi.org/10.1107/S2056989015004727 |
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author | Jeyaseelan, S. Sowmya, B. R. Venkateshappa, G. Raghavendra Kumar, P. Palakshamurthy, B. S. |
author_facet | Jeyaseelan, S. Sowmya, B. R. Venkateshappa, G. Raghavendra Kumar, P. Palakshamurthy, B. S. |
author_sort | Jeyaseelan, S. |
collection | PubMed |
description | In the title compound, C(16)H(17)NO(2)S, the heterocyclic ring adopts a half-chair conformation and the bond-angle sum at the N atom is 354.6°. The dihedral angle between the planes of the aromatic rings is 74.15 (10)°. In the crystal, molecules are linked by weak C—H⋯O hydrogen bonds, generating C(8) and C(4) chains propagating along [100] and [010], respectively, which together generate (001) sheets. |
format | Online Article Text |
id | pubmed-4438803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-44388032015-05-30 Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline Jeyaseelan, S. Sowmya, B. R. Venkateshappa, G. Raghavendra Kumar, P. Palakshamurthy, B. S. Acta Crystallogr E Crystallogr Commun Data Reports In the title compound, C(16)H(17)NO(2)S, the heterocyclic ring adopts a half-chair conformation and the bond-angle sum at the N atom is 354.6°. The dihedral angle between the planes of the aromatic rings is 74.15 (10)°. In the crystal, molecules are linked by weak C—H⋯O hydrogen bonds, generating C(8) and C(4) chains propagating along [100] and [010], respectively, which together generate (001) sheets. International Union of Crystallography 2015-03-21 /pmc/articles/PMC4438803/ /pubmed/26029439 http://dx.doi.org/10.1107/S2056989015004727 Text en © Jeyaseelan et al. 2015 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 | Data Reports Jeyaseelan, S. Sowmya, B. R. Venkateshappa, G. Raghavendra Kumar, P. Palakshamurthy, B. S. Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline |
title | Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline |
title_full | Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline |
title_fullStr | Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline |
title_full_unstemmed | Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline |
title_short | Crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline |
title_sort | crystal structure of 1-benzylsulfonyl-1,2,3,4-tetrahydroquinoline |
topic | Data Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438803/ https://www.ncbi.nlm.nih.gov/pubmed/26029439 http://dx.doi.org/10.1107/S2056989015004727 |
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