2013•The Journal of Pharmaceutical PracticeRequires access

Synthesis and antifungal activities of new triazole compounds

Pang Ta

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Abstract

Objective To design and synthesis novel triazole antifungal derivatives and study the antifungal activity.Methods All the target compounds were prepared from 1,3- difluorobenzene via click reaction;The antibacterial activities of the title compounds were determined with broth dilution method.Results Twelve compounds were synthesized and characterized by 1H NMR and MS.All the title compounds exhibited potent antifungal activities against nearly all fungi tested.Conclusion The electronic effects of the substituents affected the activity of compounds,specifically the electron- donating groups.

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Objective To design and synthesis novel triazole antifungal derivatives and study the antifungal activity.Methods All the target compounds were prepared from 1,3- difluorobenzene via click reaction;The antibacterial activities of the title compounds were determined with broth dilution method.Results Twelve compounds were synthesized and characterized by 1H NMR and MS.All the title compounds exhibited potent antifungal activities against nearly all fungi tested.Conclusion The electronic effects of the substituents affected the activity of compounds,specifically the electron- donating groups.

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Available abstract

Objective To design and synthesis novel triazole antifungal derivatives and study the antifungal activity.Methods All the target compounds were prepared from 1,3- difluorobenzene via click reaction;The antibacterial activities of the title compounds were determined with broth dilution method.Results Twelve compounds were synthesized and characterized by 1H NMR and MS.All the title compounds exhibited potent antifungal activities against nearly all fungi tested.Conclusion The electronic effects of the substituents affected the activity of compounds,specifically the electron- donating groups.

Key concepts: Antifungal, Chemistry, Triazole, Combinatorial chemistry, Click chemistry, Proton NMR, Organic chemistry, Stereochemistry

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