Cytotoxic activity of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones and 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides

6/6,7-Substituted-3-formylchromones (8a-g) were reacted with 2 equivalents thiobenzamide (9) in refluxing toluene to furnish substituted-3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones (10a-g) in high yields. Similarly, when substituted-2-anilino-3-formylchromones (8a-d) were reacted with thiobe...

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Veröffentlicht in:European journal of medicinal chemistry 2010-02, Vol.45 (2), p.790-794
Hauptverfasser: RAJ, Tilak, RICHA KAUR BHATIA, KAPUR, Ashish, SHARMA, Madhunika, SAXENA, A. K, ISHAR, M. P. S
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Sprache:eng
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