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rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one
In the title compound, C(22)H(21)NOS, the thiopyranone ring adopts a chair-like conformation with the substituent in the axial position. The relative configuration of the racemic compound is 3R,7S according to the numbering scheme used in this publication. In the crystal packing, centrosymmetric d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295517/ https://www.ncbi.nlm.nih.gov/pubmed/22412628 http://dx.doi.org/10.1107/S1600536812005983 |
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author | Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid |
author_facet | Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid |
author_sort | Harms, Klaus |
collection | PubMed |
description | In the title compound, C(22)H(21)NOS, the thiopyranone ring adopts a chair-like conformation with the substituent in the axial position. The relative configuration of the racemic compound is 3R,7S according to the numbering scheme used in this publication. In the crystal packing, centrosymmetric dimers are built up via N—H⋯O hydrogen bonds, with graph set R (2) (2)(8). |
format | Online Article Text |
id | pubmed-3295517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32955172012-03-12 rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(22)H(21)NOS, the thiopyranone ring adopts a chair-like conformation with the substituent in the axial position. The relative configuration of the racemic compound is 3R,7S according to the numbering scheme used in this publication. In the crystal packing, centrosymmetric dimers are built up via N—H⋯O hydrogen bonds, with graph set R (2) (2)(8). International Union of Crystallography 2012-02-17 /pmc/articles/PMC3295517/ /pubmed/22412628 http://dx.doi.org/10.1107/S1600536812005983 Text en © Harms et al. 2012 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 Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one |
title |
rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one |
title_full |
rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one |
title_fullStr |
rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one |
title_full_unstemmed |
rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one |
title_short |
rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one |
title_sort | rac-3-[(anilino)(naphthalen-2-yl)methyl]thian-4-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295517/ https://www.ncbi.nlm.nih.gov/pubmed/22412628 http://dx.doi.org/10.1107/S1600536812005983 |
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