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Russian Journal of Organic Chemistry

, Volume 50, Issue 7, pp 1022–1027 | Cite as

Protonation, deuteration, and formylation of aceperidazylenes

  • V. V. Mezheritskii
  • L. G. Minyaeva
  • N. I. Omelichkin
  • A. A. Milov
  • K. A. Lysenko
  • A. F. Smolyakov
Article

Abstract

1H-1,2-Diazaphenalene derivatives in which the pyridazine ring is ortho- and peri-fused to acenaphthene and acenaphthylene (1H-indeno[6,7,1-def]cinnolines) have been synthesized. It has been found that electrophilic attack on these compounds is directed at C6.

Keywords

Acenaphthene Electrophilic Attack Acenaphthylene Naphthalene Ring Cinnoline 
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

© Pleiades Publishing, Ltd. 2014

Authors and Affiliations

  • V. V. Mezheritskii
    • 1
  • L. G. Minyaeva
    • 1
  • N. I. Omelichkin
    • 1
  • A. A. Milov
    • 2
  • K. A. Lysenko
    • 3
  • A. F. Smolyakov
    • 3
  1. 1.Research Institute of Physical and Organic ChemistrySouthern Federal UniversityRostov-on-DonRussia
  2. 2.Southern Scientific CenterRussian Academy of SciencesRostov-on-DonRussia
  3. 3.Nesmeyanov Institute of Organoelement CompoundsRussian Academy of SciencesMoscowRussia

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