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4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one
In the title compound, C(21)H(23)NOS, the thiazolidine ring adopts a twist conformation about one of its C—S bonds, while the cyclohexane ring has a chair conformation. The S and N atoms attached to the spiro C atom are in axial and equatorial orientations, respectively. The thiazolidine ring for...
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/PMC3344557/ https://www.ncbi.nlm.nih.gov/pubmed/22590319 http://dx.doi.org/10.1107/S1600536812015358 |
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author | Fun, Hoong-Kun Chia, Tze Shyang Shanmugavelan, Poovan Ponnuswamy, Alagusundaram |
author_facet | Fun, Hoong-Kun Chia, Tze Shyang Shanmugavelan, Poovan Ponnuswamy, Alagusundaram |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | In the title compound, C(21)H(23)NOS, the thiazolidine ring adopts a twist conformation about one of its C—S bonds, while the cyclohexane ring has a chair conformation. The S and N atoms attached to the spiro C atom are in axial and equatorial orientations, respectively. The thiazolidine ring forms dihedral angles of 86.24 (14) and 31.82 (15)° with the directly attached and remote terminal benzene rings, respectively. The dihedral angle between the two terminal benzene rings is 86.74 (14)°. In the crystal, the only significant directional interaction is a weak C—H⋯π bond, which generates [010] chains. |
format | Online Article Text |
id | pubmed-3344557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33445572012-05-15 4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one Fun, Hoong-Kun Chia, Tze Shyang Shanmugavelan, Poovan Ponnuswamy, Alagusundaram Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(23)NOS, the thiazolidine ring adopts a twist conformation about one of its C—S bonds, while the cyclohexane ring has a chair conformation. The S and N atoms attached to the spiro C atom are in axial and equatorial orientations, respectively. The thiazolidine ring forms dihedral angles of 86.24 (14) and 31.82 (15)° with the directly attached and remote terminal benzene rings, respectively. The dihedral angle between the two terminal benzene rings is 86.74 (14)°. In the crystal, the only significant directional interaction is a weak C—H⋯π bond, which generates [010] chains. International Union of Crystallography 2012-04-18 /pmc/articles/PMC3344557/ /pubmed/22590319 http://dx.doi.org/10.1107/S1600536812015358 Text en © Fun 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 Fun, Hoong-Kun Chia, Tze Shyang Shanmugavelan, Poovan Ponnuswamy, Alagusundaram 4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one |
title | 4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one |
title_full | 4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one |
title_fullStr | 4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one |
title_full_unstemmed | 4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one |
title_short | 4-Benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one |
title_sort | 4-benzyl-8-phenyl-1-thia-4-azaspiro[4.5]decan-3-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344557/ https://www.ncbi.nlm.nih.gov/pubmed/22590319 http://dx.doi.org/10.1107/S1600536812015358 |
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