• 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