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
Record number
2624408
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