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peri Annelation of Perimidines in Reactions with 1,3-Dicarbonyl Compounds*

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Chemistry of Heterocyclic Compounds Aims and scope

An Erratum to this article was published on 01 May 2016

A new approach to 1,3-diazapyrenes via peri annelation of perimidines with 1,3-dicarbonyl compounds is developed. It is demonstrated that this method has a number of advantages compared to a previously reported procedure employing chalcones as electrophilic components. The new method can be used for efficient double peri annelation of biperimidines with 1,3-dicarbonyl compounds affording 2,2′-bi-1,3-diazapyrenes.

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This work was financially supported by the Russian Scientific Fund (grant 14-23-00068).

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Authors and Affiliations

  1. North Caucasus Federal University, 1a Pushkina St., Stavropol, 355009, Russia

    A. V. Aksenov, M. H. Magamadova, D. A. Lobach, I. V. Aksenova & I. V. Malikova

  2. Department of Chemistry, University of Kansas, 1255 Wescoe Hall Drive, Lawrence, KS, 66049, USA

    M. Rubin

Authors
  1. A. V. Aksenov
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  2. M. H. Magamadova
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  3. D. A. Lobach
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  4. I. V. Aksenova
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  5. I. V. Malikova
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  6. M. Rubin
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Correspondence to A. V. Aksenov.

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*Dedicated to Academician Yurii Nikolaevich Bubnov on the occasion of his 80th birthday and in memory of working together.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1408-1415, September, 2014.

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Aksenov, A.V., Magamadova, M.H., Lobach, D.A. et al. peri Annelation of Perimidines in Reactions with 1,3-Dicarbonyl Compounds*. Chem Heterocycl Comp 50, 1298–1304 (2014). https://doi.org/10.1007/s10593-014-1592-2

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  • DOI: https://doi.org/10.1007/s10593-014-1592-2

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