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Methyl 2,6-diphenyl-1-p-tolyl-4-(p-tolyl- amino)-1,2,5,6-tetrahydropyridine-3- carboxylate

dc.contributor.authorVenugopala, Katharigatta Narayanaswamyen_US
dc.contributor.authorNayak, Susanta K.en_US
dc.contributor.authorOdhav, Bhartien_US
dc.date.accessioned2012-11-07T07:51:40Z
dc.date.available2012-11-07T07:51:40Z
dc.date.issued2012
dc.descriptionOriginally published in: Acta Cryst.; Vol. 68, Pt 8, 2012.en_US
dc.description.abstractIn the title compound, C33H32N2O2, the tetrahydropyridine ring adopts a boat conformation with the carbonyl group in an s-cis conformation with respect to the C=C bond of the six-membered tetrahydropyridine ring. The molecular conformation is stabilized by intramolecular N-H...O, C-H...O and C-H...[pi] interactions. Formation of centrosymmetric head-to-head dimers is observed through pairwise intermolecular N-H...O hydrogen bonds. Additional weak C-H...O and C-H...[pi] interactions stabilize the three-dimensional molecular assembly.en_US
dc.dut-rims.pubnumDUT-001724en_US
dc.format.extent13 p.en_US
dc.identifier.citationVenugopala, K. N., Nayak, S. K. & Odhav, B. (2012). Acta Cryst. E68, o2392-o2393.en_US
dc.identifier.doi10.1107/S1600536812030309
dc.identifier.urihttp://hdl.handle.net/10321/776
dc.language.isoenen_US
dc.publisherActa Cryst.en_US
dc.publisher.urihttp://journals.iucr.org/e/issues/2012/08/00/zl2490/index.htmlen_US
dc.rightsThis open-access article is distributed under the terms of the Creative Commons Attribution Licence http://creativecommons.org/licenses/by/2.0/uk/legalcode, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.en_US
dc.subject.lcshOrganic compundsen_US
dc.subject.lcshMethylphenyltetrahydropyridineen_US
dc.subject.lcshPiperidine—Derivativesen_US
dc.titleMethyl 2,6-diphenyl-1-p-tolyl-4-(p-tolyl- amino)-1,2,5,6-tetrahydropyridine-3- carboxylateen_US
dc.typeArticleen_US

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