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Synthesis and spectroscopic properties of novel benzo[a]phenanthridines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Condensation of arylidene-2-naphthylarnines with 5,5-dimethylcyclohexane-1,3-dione (dimedone) gives novel 2,2-dimethyl-5-R-1,2,3,4,5,6-hexahydrobenzo[a]phenanthridin-4-ones. Treatment of azomethines containing an ortho hydroxyl group in the “aldehyde” fragment gives the corresponding 3,3,6,6-tetramethyl-9-R-1,2,3,4,5,6,7,8-octa-hydroxanthene-1,8-diones. The IR, UV, PMR, and mass spectra of the compounds synthesized have been studied.

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Authors and Affiliations

  1. Belorussian Institute of Physicoorganic Chemistry, 220603, Minsk

    N. G. Kozlov, K. N. Gusak & S. A. Makhnach

Authors
  1. N. G. Kozlov
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  2. K. N. Gusak
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  3. S. A. Makhnach
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Kozlov, N.G., Gusak, K.N. & Makhnach, S.A. Synthesis and spectroscopic properties of novel benzo[a]phenanthridines. Chem Heterocycl Compd 32, 30–34 (1996). https://doi.org/10.1007/BF01169349

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  • DOI: https://doi.org/10.1007/BF01169349

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