Title of article :
Synthesis and crystal structures of a bis­­(3-hy­dr­oxy-cyclo­hex-2-en-1-one) and two hexa­hydro­quinoline derivatives
Author/Authors :
Steiger, Scott A. Department of Biomedical and Pharmaceutical Sciences - The University of Montana, USA , Li, Chun Department of Chemistry - Ithaca College, USA , Gates, Christina Department of Biomedical and Pharmaceutical Sciences - The University of Montana, USA , Natale, Nicholas R. Department of Biomedical and Pharmaceutical Sciences - The University of Montana, USA
Pages :
26
From page :
1
To page :
26
Abstract :
The title compound I, 2,20 -[(2-nitrophenyl)methylene]bis(3-hydroxy-5,5-dimethylcyclohex-2-enone), C23H27NO6, features a 1,3-ketone–enol conformation which is stabilized by two intramolecular hydrogen bonds. The most prominent intermolecular interactions in compound I are C—HO hydrogen bonds, which link molecules into a two-dimensional network parallel to the (001) plane and a chain perpendicular to (111). Both title compounds II, ethyl 4-(4-hydroxy3,5-dimethoxyphenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3- carboxylate, C23H29NO6, and III, ethyl 4-(anthracen-9-yl)-2,7,7-trimethyl-5-oxo1,4,5,6,7,8-hexahydroquinoline-3-carboxylate, C29H29NO3, share the same structural features, such as a shallow boat conformation of the dihydropyridine group and an orthogonal aryl group attached to the dihydropyridine. Intermolecular N—HO bonding is present in the crystal packing of both compound II and III.
Keywords :
crystal structure , hexa­hydro­quinoline , hydrogen bonding
Journal title :
Acta Crystallographica Section E: Crystallographic Communications
Serial Year :
2020
Full Text URL :
Record number :
2624408
Link To Document :
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