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dc.contributor.authorGündüz, Miyase Gözde
dc.contributor.authorButcher, Ray J.
dc.contributor.authorÖztürk Yildirim, Sema
dc.contributor.authorEl-Khouly, Ahmed
dc.contributor.authorŞafak, Cihat
dc.contributor.authorŞimşek, Rahime
dc.date.accessioned2019-12-16T10:09:48Z
dc.date.available2019-12-16T10:09:48Z
dc.date.issued2012
dc.identifier.issn1600-5368
dc.identifier.urihttps://doi.org/10.1107/S1600536812046909
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588994/
dc.identifier.urihttp://hdl.handle.net/11655/19973
dc.description.abstractThe title compound, C23H25BrN2O3, crystallizes with two independent mol­ecules in the asymmetric unit (Z′ = 2) which differ in the twist of the 5-bromo-1H-indole ring with respect to the plane of the 4-methyl-1,4,5,6,7,8-hexa­hydro­quinoline ring [dihedral angles of 78.55 (9) and 89.70 (8)° in molecules A and B, respectively]. The indole ring is planar in both molecules [maximum deviations = 0.021 (3) and −0.020 (3) Å for the N atom] while the cyclo­hexene ring has adopts a sofa conformation. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming dimers with R 1 2(6) ring motifs. These dimers are connected by N—H⋯O hydrogen bonds, generating chains along [110]. A C—H⋯O contact occurs between the independent mol­ecules.
dc.relation.isversionof10.1107/S1600536812046909
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleEthyl 4-(5-Bromo-1H-Indol-3-Yl)-2,6,6-Trimethyl-5-Oxo-1,4,5,6,7,8-Hexa­Hydro­Quinoline-3-Carboxyl­Ate
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalActa Crystallographica Section E: Structure Reports Online
dc.contributor.departmentFarmasötik Kimya
dc.identifier.volume68
dc.identifier.issuePt 12
dc.identifier.startpageo3404
dc.identifier.endpageo3405
dc.description.indexPubMed
dc.description.indexScopus


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