Abstract

A series of some 6H-thiochromeno[4,3-b]quinoline derivatives were prepared by the reaction of
4-chloro-2H-thiochromene-3-carbaldehydes with 2-aminophenols in DMF and characterized by analytical and spectral
methods. All the compounds under test were found to be active against M.gypseum and E.floccosum higher than that of
the standard fluconazole.

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