Issue 5, 1997
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Synthesis and biological testing of pyrano[2,3-a]acridinones

Jacqueline A. Drewe  and  Paul W. Groundwater  

Abstract

The synthesis of 12-amino- 7a and 12-hydroxy-2-arylpyrano[2,3-a]acridin-4-ones 7b and 19 via the von Strandtmann flavone annelation procedure is described, in which the pyranone ring is formed by the reaction of a β-ketosulfoxide 13, 18 with an aromatic aldehyde.

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Article information

DOI
https://doi.org/10.1039/A606689E
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 601-606

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Synthesis and biological testing of pyrano[2,3-a]acridinones

J. A. Drewe and P. W. Groundwater, J. Chem. Soc., Perkin Trans. 1, 1997, 601 DOI: 10.1039/A606689E

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