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Vanillin esters of aromatic carboxylic acids in the synthesis of benzo[a]acridine and benzo[b][4,7]phenanthroline derivatives

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Abstract

By condensation of vanillin esters of substituted benzoic acids with 2-naphthylamine and 6-quinolylamines and also with cyclic β-diketones (1,3-cyclohexanedione and dimedone) 2-methoxy-4-(11-oxo-7,8,9,10,11,12-hexahydrobenzo[a]acridin-12-yl)-and 2-methoxy-4-(11-oxo-7,8,9,10,11,12-hexahydrobenzo[b][4,7]-phenanthrolin-12-yl)phenyl benzoates were prepared.

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Authors and Affiliations

  1. Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus, Minsk, 220072, Belarus

    N. G. Kozlov, A. B. Tereshko & K. N. Gusak

Authors
  1. N. G. Kozlov
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  2. A. B. Tereshko
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  3. K. N. Gusak
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Correspondence to N. G. Kozlov.

Additional information

Original Russian Text © N.G. Kozlov, A.B. Tereshko, K.N. Gusak, 2006, published in Zhurnal Organicheskoi Khimii, 2006, Vol. 42, no. 2, pp. 281–287.

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Kozlov, N.G., Tereshko, A.B. & Gusak, K.N. Vanillin esters of aromatic carboxylic acids in the synthesis of benzo[a]acridine and benzo[b][4,7]phenanthroline derivatives. Russ J Org Chem 42, 266–272 (2006). https://doi.org/10.1134/S1070428002120199

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  • DOI: https://doi.org/10.1134/S1070428002120199

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