1,4-Bis-(piperidin-1-ylcarbonyl)benzene
| File | Size | Format | |
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| 50296__1.pdf | 288Kb | Adobe PDF | View |
| Title | 1,4-Bis-(piperidin-1-ylcarbonyl)benzene |
|---|---|
| Author | Armbrust, Lee; Bilyk, Alex; Brown, Chris; Healy, Peter Conrad |
| Journal Name | Acta Crystallographica. Section E: Structure reports online |
| Year Published | 2008 |
| Place of publication | Denmark |
| Publisher | Blackwell Munksgaard |
| Abstract | The title compound, C18H20N2O2, has been synthesized by the reaction of terephthaloyl chloride and 1,2,3,6-tetrahydropyridine. This compound crystallizes as discrete molecular species disposed about a crystallographic centre of symmetry, such that half the molecule constitutes the asymmetric unit. The structure shows an envelope conformation for the dehydropiperidine ring with the amide carbonyl twisted out of the benzene ring plane by 57.3 (2)°. |
| Peer Reviewed | Yes |
| Published | Yes |
| Publisher URI | http://journals.iucr.org/e/journalhomepage.html |
| Alternative URI | http://dx.doi.org/10.1107/S1600536807062423 |
| Copyright Statement | Copyright remains with the authors 2008. For information about this journal please refer to the journal's website. All articles published in Acta Crystallographica Section E are open access and distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. See http://creativecommons.org/licenses/by/2.0/uk/legalcode |
| Volume | E64 |
| Page from | o31 |
| Page to | o31 |
| ISSN | 1600-5368 |
| Date Accessioned | 2008-06-13 |
| Date Available | 2009-08-20T07:01:13Z |
| Language | en_AU |
| Research Centre | Queensland Micro and Nanotechnology Centre; Eskitis Institute for Drug Discovery |
| Faculty | Faculty of Science, Environment, Engineering and Technology |
| Subject | PRE2009-Structural Chemistry |
| URI | http://hdl.handle.net/10072/20167 |
| Publication Type | Journal Articles (Refereed Article) |
| Publication Type Code | c1 |
Please use this identifier to cite this record: http://hdl.handle.net/10072/20167
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