Abstract
A number of quinoline N-oxides have been prepared and oxidized by means of lead tetraacetate to quinoline hydroxamic acids (i.e. derivatives of 1-hydroxy-2(1H)-quinolone). Contrary to the findings of other investigators, 1-hydroxy-4-nitro-2(1H)-quinolone (2e) is obtained by treating 4-nitroquinoline 1-oxide with lead tetraacetate. Quinolines with a methyl group in the 8-position could not be oxidized to N-oxides with hydrogen peroxide.The antibacterial properties of the hydroxamic acids and some of the N-oxides were evaluated against S. aureus and E. coli.
Cite
CITATION STYLE
Coutts, R. T., Hindmarsh, K. W., & Myers, G. E. (1970). Quinoline N -oxides and hydroxamic acids with antibacterial properties. Canadian Journal of Chemistry, 48(15), 2393–2396. https://doi.org/10.1139/v70-400
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