Chemistry of Heterocyclic Compounds

, Volume 23, Issue 4, pp 426–435 | Cite as

Imidazoline ring cleavage in 1,3,6,10-tetraazatetracyclo-[7.3.1.02,7.06,13]trideca-4, 11-dienes, leading to the formation of diquinoxalino[1,2-a∶2′,3′-d]pyrrole derivatives

  • V. N. Charushin
  • G. M. Petrova
  • G. G. Aleksandrov
  • L. G. Egorova
  • A. I. Chernishev
  • E. O. Sidorov
  • N. A. Klyuev
  • O. N. Chupakhin
Article
  • 27 Downloads

Abstract

Dibenzo[d,k]-1,3,6,10-tetraazatetracyclo[7.3.1.02,7.06,13]trideca-4,11-dienes undergo addition reactions at the C(2) carbon atom with alcohols and thiols, accompanied by cleavage of the C-N bond of the imidazoline ring, to generate diquinoxalino[1,2-a∶2′,3′-d]pyrrole derivatives.

Keywords

Alcohol Organic Chemistry Carbon Atom Thiol Diene 

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Copyright information

© Plenum Publishing Corporation 1987

Authors and Affiliations

  • V. N. Charushin
    • 1
  • G. M. Petrova
    • 1
  • G. G. Aleksandrov
    • 1
  • L. G. Egorova
    • 1
  • A. I. Chernishev
    • 1
  • E. O. Sidorov
    • 1
  • N. A. Klyuev
    • 1
  • O. N. Chupakhin
    • 1
  1. 1.S. M. Kirov Ural Polytechnical InstituteSverdlovsk

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