rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one
In the title compound, C22H21NOS, 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...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2012-03-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536812005983 |
| _version_ | 1818322205920985088 |
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| author | A. Wahid Mesbah Mohammad M. Mojtahedi Klaus Harms M. Saeed Abaee |
| author_facet | A. Wahid Mesbah Mohammad M. Mojtahedi Klaus Harms M. Saeed Abaee |
| author_sort | A. Wahid Mesbah |
| collection | DOAJ |
| description | In the title compound, C22H21NOS, 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 R22(8). |
| first_indexed | 2024-12-13T10:53:06Z |
| format | Article |
| id | doaj.art-ae26bff3797241bba4d6b8403f25a5b1 |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-13T10:53:06Z |
| publishDate | 2012-03-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-ae26bff3797241bba4d6b8403f25a5b12022-12-21T23:49:45ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-03-01683o749o74910.1107/S1600536812005983rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-oneA. Wahid MesbahMohammad M. MojtahediKlaus HarmsM. Saeed AbaeeIn the title compound, C22H21NOS, 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 R22(8).http://scripts.iucr.org/cgi-bin/paper?S1600536812005983 |
| spellingShingle | A. Wahid Mesbah Mohammad M. Mojtahedi Klaus Harms M. Saeed Abaee rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one Acta Crystallographica Section E |
| 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 |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536812005983 |
| work_keys_str_mv | AT awahidmesbah rac3anilinonaphthalen2ylmethylthian4one AT mohammadmmojtahedi rac3anilinonaphthalen2ylmethylthian4one AT klausharms rac3anilinonaphthalen2ylmethylthian4one AT msaeedabaee rac3anilinonaphthalen2ylmethylthian4one |