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Protonation, deuteration, and formylation of aceperidazylenes

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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.

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Authors and Affiliations

  1. Research Institute of Physical and Organic Chemistry, Southern Federal University, pr. Stachki 194/2, Rostov-on-Don, 344090, Russia

    V. V. Mezheritskii, L. G. Minyaeva & N. I. Omelichkin

  2. Southern Scientific Center, Russian Academy of Sciences, ul. Chekhova 41, Rostov-on-Don, 344006, Russia

    A. A. Milov

  3. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Moscow, 119991, Russia

    K. A. Lysenko & A. F. Smolyakov

Authors
  1. V. V. Mezheritskii
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  2. L. G. Minyaeva
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  3. N. I. Omelichkin
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  4. A. A. Milov
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  5. K. A. Lysenko
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  6. A. F. Smolyakov
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Corresponding author

Correspondence to L. G. Minyaeva.

Additional information

Original Russian Text © V.V. Mezheritskii, L.G. Minyaeva, N.I. Omelichkin, A.A. Milov, K.A. Lysenko, A.F. Smolyakov, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 7, pp. 1038–1043.

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Mezheritskii, V.V., Minyaeva, L.G., Omelichkin, N.I. et al. Protonation, deuteration, and formylation of aceperidazylenes. Russ J Org Chem 50, 1022–1027 (2014). https://doi.org/10.1134/S107042801407015X

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  • DOI: https://doi.org/10.1134/S107042801407015X

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