2003•Zhongguo yaowu huaxue zazhiRequires access

Syntheses and the antifungal activity of 3-bromo-4-thiochrom(an)ones

Qi Ping

Open publisher page 4 citations

Abstract

Aim To design and synthesize the 3-bromo-4-thiochrom(an)ones,and to value their antifungal activity. Methods BZ] The target compounds were prepared from the thiochromanones through bromination and oxidation,their antifungal effects were tested in vitro . Results Nine new compounds were synthesized.The structures of these compounds were confirmed by IR, 1H-NMR and elemental analyses.The compound The target compounds were prepared from the thiochromanones through bromination and oxidation,their antifungal effects were tested in vitro . Results Nine new compounds were synthesized.The structures of these compounds were confirmed by IR, 1H-NMR and elemental analyses.The compound Ⅴ_b exhibited excellent antifungal activity.Its MIC value was below or equal to that of the control. Conclusion The 3-bromo substituted thiochromanones show potent antifungal activity.

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What this paper is about

Aim To design and synthesize the 3-bromo-4-thiochrom(an)ones,and to value their antifungal activity. Methods BZ] The target compounds were prepared from the thiochromanones through bromination and oxidation,their antifungal effects were tested in vitro . Results Nine new compounds were synthesized.The structures of these compounds were confirmed by IR, 1H-NMR and elemental analyses.The compound The target compounds were prepared from the thiochromanones through bromination and oxidation,their antifungal effects were tested in vitro . Results Nine new compounds were synthesized.The structures of these compounds were confirmed by IR, 1H-NMR and elemental analyses.The compound Ⅴ_b exhibited excellent antifungal activity.Its MIC value was below or equal to that of the control. Conclusion The 3-bromo substituted thiochromanones show potent antifungal activity.

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Available abstract

Aim To design and synthesize the 3-bromo-4-thiochrom(an)ones,and to value their antifungal activity. Methods BZ] The target compounds were prepared from the thiochromanones through bromination and oxidation,their antifungal effects were tested in vitro . Results Nine new compounds were synthesized.The structures of these compounds were confirmed by IR, 1H-NMR and elemental analyses.The compound The target compounds were prepared from the thiochromanones through bromination and oxidation,their antifungal effects were tested in vitro . Results Nine new compounds were synthesized.The structures of these compounds were confirmed by IR, 1H-NMR and elemental analyses.The compound Ⅴ_b exhibited excellent antifungal activity.Its MIC value was below or equal to that of the control. Conclusion The 3-bromo substituted thiochromanones show potent antifungal activity.

Key concepts: Antifungal, Chemistry, Halogenation, Proton NMR, In vitro, Elemental analysis, Carbon-13 NMR, Stereochemistry

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