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Vanilline Alkanoates in the Synthesis of Hexahydrobenzacridine and Octahydroxanthene Derivatives

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Abstract

Cascade heterocyclization of 1,3-cyclohexanedione and dimedone with 2-naphthylamine and vanilline esters gave derivatives of 2-methoxy-4-(alkyl-11-oxo-7,8,9,10,11,12-hexahydrobenz[a]acridin-12-yl)- and 2-methoxy-4-(alkyl-1,8-dioxo-2,3,4,5,6,7,8,9-octahydro-1H-xanthen-9-yl)phenyl esters of aliphatic (C1– C4 ) carboxylic acids.

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Authors and Affiliations

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

    N. G. Kozlov & L. I. Basalaeva

Authors
  1. N. G. Kozlov
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  2. L. I. Basalaeva
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Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 4, 2005, pp. 654–658.

Original Russian Text Copyright © 2005 by Kozlov, Basalaeva.

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Kozlov, N.G., Basalaeva, L.I. Vanilline Alkanoates in the Synthesis of Hexahydrobenzacridine and Octahydroxanthene Derivatives. Russ J Gen Chem 75, 617–621 (2005). https://doi.org/10.1007/s11176-005-0282-2

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  • DOI: https://doi.org/10.1007/s11176-005-0282-2

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