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Russian Journal of Organic Chemistry

, Volume 41, Issue 5, pp 727–734 | Cite as

Phendione in the Synthesis of Annelated Derivatives of 4,7-Phenanthroline

  • K. N. Gusak
  • A. B. Tereshko
  • N. G. Kozlov
Article

Abstract

By condensation of 5-phenyl-1,3-cyclohexanedione with 6-quinolylamine and aldehydes of aromatic, heterocyclic, and cyclohexene series new 12-aryl(heteryl, cyclohexenyl)-9-phenyl-8,9,10,12-tetrahydro-7H-benzo[b][4,7]phenanthrolin-11-ones were prepared. The presence of diastereomers in the target reaction products was determined by 1H NMR spectroscopy.

Keywords

Spectroscopy Organic Chemistry Aldehyde Cyclohexanedione Target Reaction 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© MAIK “Nauka/Interperiodica” 2005

Authors and Affiliations

  • K. N. Gusak
    • 1
  • A. B. Tereshko
    • 1
  • N. G. Kozlov
    • 1
  1. 1.Institute of Physical Organic ChemistryNational Academy of Sciences of BelarusMinskBelarus

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