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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...

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Autores principales: Harms, Klaus, Abaee, M. Saeed, Mojtahedi, Mohammad M., Mesbah, A. Wahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
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).
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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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