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

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dc.contributor.author Venugopala, Katharigatta Narayanaswamy
dc.contributor.author Nayak, Susanta K.
dc.contributor.author Odhav, Bharti
dc.date.accessioned 2012-11-07T07:51:40Z
dc.date.available 2012-11-07T07:51:40Z
dc.date.issued 2012
dc.identifier.citation Venugopala, K. N., Nayak, S. K. & Odhav, B. (2012). Acta Cryst. E68, o2392-o2393. en_US
dc.identifier.uri http://hdl.handle.net/10321/776
dc.description Originally published in: Acta Cryst.; Vol. 68, Pt 8, 2012. en_US
dc.description.abstract In 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.format.extent 13 p. en_US
dc.language.iso en en_US
dc.publisher Acta Cryst. en_US
dc.rights This 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.lcsh Organic compunds en_US
dc.subject.lcsh Methylphenyltetrahydropyridine en_US
dc.subject.lcsh Piperidine—Derivatives en_US
dc.title Methyl 2,6-diphenyl-1-p-tolyl-4-(p-tolyl- amino)-1,2,5,6-tetrahydropyridine-3- carboxylate en_US
dc.type Article en_US
dc.publisher.uri http://journals.iucr.org/e/issues/2012/08/00/zl2490/index.html en_US
dc.dut-rims.pubnum DUT-001724


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