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


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.


Spectroscopy Organic Chemistry Aldehyde Cyclohexanedione Target Reaction 
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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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