chemistry Department, Faculty of Science, Sohag University, 82524 Sohag, Egypt.
10.18576/jpac/020307
Abstract
Classes of novel sulfonylurea and sulfonamide derivatives 3-13 were synthesized via three different roots, using pharmacologically active functionalized pyrimidine or piperidine-2,6-dione derivatives and p-toluene sulfonyl chloride under phase transfer conditions (PTC). The structures of all the newly synthesized compounds were characterized by IR, 1H-NMR and 13C-NMR spectroscopy. The title compounds were screened for antibacterial activity against two-gram positive bacterial strains such as Staphylococcus aureus and Bacillus subtilis and two-gram negative bacterial strains such as Escherichia coli and Pseudomonas aeruginosa and also screened for antifungal activity against Fusarium oxysporum, Candida albicans and Aspergillus niger pathogens. Compounds 3b, 4b, 6b, 6d, 8b, 11b, 13b and 13e exhibited potent activity and remaining derivatives showed moderate to weak activity against bacteria and fungi
A. A. Mohamed, M., G. A. Tamam, M., & El-Saghier, M. M. (2016). Synthesis and Biological Evaluation of Some Novel Sulfonylurea and Sulfonamide Derivatives under Phase Transfer Catalysis Conditions. Journal of Pharmaceutical and Applied Chemistry, 2(3), 66-73. doi: 10.18576/jpac/020307
MLA
Mounir A. A. Mohamed; Maha G. A. Tamam; M. M. El-Saghier. "Synthesis and Biological Evaluation of Some Novel Sulfonylurea and Sulfonamide Derivatives under Phase Transfer Catalysis Conditions". Journal of Pharmaceutical and Applied Chemistry, 2, 3, 2016, 66-73. doi: 10.18576/jpac/020307
HARVARD
A. A. Mohamed, M., G. A. Tamam, M., El-Saghier, M. M. (2016). 'Synthesis and Biological Evaluation of Some Novel Sulfonylurea and Sulfonamide Derivatives under Phase Transfer Catalysis Conditions', Journal of Pharmaceutical and Applied Chemistry, 2(3), pp. 66-73. doi: 10.18576/jpac/020307
VANCOUVER
A. A. Mohamed, M., G. A. Tamam, M., El-Saghier, M. M. Synthesis and Biological Evaluation of Some Novel Sulfonylurea and Sulfonamide Derivatives under Phase Transfer Catalysis Conditions. Journal of Pharmaceutical and Applied Chemistry, 2016; 2(3): 66-73. doi: 10.18576/jpac/020307
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