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TÜBİTAK

Turkish Journal of Chemistry

Journal

2016

Thiazole

Articles 1 - 2 of 2

Full-Text Articles in Physical Sciences and Mathematics

Synthesis Of Novel Thiazolylpyrazoline Derivatives And Evaluation Of Their Antimicrobial Activities And Cytotoxicities, Aouatef Tabbi, Zafer Asim Kaplancikli, Dahmane Tebbani, Leyla Yurttaş, Zerri̇n Cantürk, Özlem Atli, Merve Baysal, Gülhan Turan Zitouni Jan 2016

Synthesis Of Novel Thiazolylpyrazoline Derivatives And Evaluation Of Their Antimicrobial Activities And Cytotoxicities, Aouatef Tabbi, Zafer Asim Kaplancikli, Dahmane Tebbani, Leyla Yurttaş, Zerri̇n Cantürk, Özlem Atli, Merve Baysal, Gülhan Turan Zitouni

Turkish Journal of Chemistry

Several novel thiazolylpyrazoline derivatives were synthesized by reacting substituted 3,5-diaryl-1-thiocarba\-moyl-2-pyrazolines with phenacylbromides. The structures of the synthesized compounds were confirmed by IR, $^{1}$H NMR, $^{13}$C NMR, and MS spectral data. Their antimicrobial activities against Staphylococcus aureus(ATCC-25923), Enterococcus faecalis} (ATCC-29212), Enterococcus faecalis (ATCC-51922), Listeria monocytogenes (ATCC-1911), Klebsiella pneumoniae (ATCC-700603), Pseudomonas aeruginosa (ATCC-27853), Escherichia coli (ATCC-35218), Escherichia coli (ATCC-25922), Candida albicans (ATCC-90028), Candida glabrata (ATCC-90030), Candida krusei (ATCC-6258), and Candida parapsilosis (ATCC-22019) were investigated. The compounds were also studied for their cytotoxic effects using a MTT assay. Compound 7c showed the highest antimicrobial activity, possessing the same potential as chloramphenicol against K. …


Synthetic Access To Some New Benzothiazole-Based 1,3,4-Thiadiazole And 1,3-Thiazole Derivatives, Kamal M. Dawood, Eman A. Ragab, Korany A. Ali Jan 2016

Synthetic Access To Some New Benzothiazole-Based 1,3,4-Thiadiazole And 1,3-Thiazole Derivatives, Kamal M. Dawood, Eman A. Ragab, Korany A. Ali

Turkish Journal of Chemistry

1-(Benzothiazol-2-yl)-3-phenylthiourea\textbf{ 2} was prepared and treated with hydrazonoyl chlorides \textbf{3a}--\textbf{e }to yield the corresponding 5-(benzothiazol-2-ylimino)-1,3,4-thiadiazole derivatives \textbf{6a}--\textbf{e}, respectively. Reaction of the thiourea derivative \textbf{2} with ethyl 2-chloro-3-oxobutanoate \textbf{9} afforded the corresponding 2-(benzothiazol-2-ylimino)thiazole-5-carboxylate derivative \textbf{11}. The newly synthesized heterocyclic derivatives were confirmed from their elemental and spectral analyses.