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Vanillal Esters in Reaction with 2-Naphthylamine and 1,3-Diketones

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Abstract

Analogs of natural alkaloids of acridone series, derivatives of4-(9-alkyl-11-oxo-7,8,9,10,1,12-hexahydrobenzo[a]acridin-12-yl) and 4-(12-oxo-12H-benzo[f]indeno[1,2-b]quinolin-13-yl)2-ethoxyphenyl carboxylates were synthesized by a three-component condensation of vanillal with 2-naphthylamine and 1,3-cyclohexanedione, dimedone, phendione, or 1,3-indanedione.

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Authors and Affiliations

  1. Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus, Minsk, 22007, Belarus

    N. G. Kozlov, L. I. Basalaeva & E. A. Dikusar

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  1. N. G. Kozlov
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  2. L. I. Basalaeva
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  3. E. A. Dikusar
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Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 11, 2005, pp. 1671–1680.

Original Russian Text Copyright © 2005 by Kozlov, Basalaeva, Dikusar.

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Kozlov, N.G., Basalaeva, L.I. & Dikusar, E.A. Vanillal Esters in Reaction with 2-Naphthylamine and 1,3-Diketones. Russ J Org Chem 41, 1637–1646 (2005). https://doi.org/10.1007/s11178-006-0011-2

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  • DOI: https://doi.org/10.1007/s11178-006-0011-2

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