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Full-Text Articles in Physical Sciences and Mathematics
Synthesis And Antimicrobial Evaluation Of Some New 2-(2-(P-Chlorophenyl) Benzimidazol-1-Yl Methyl)-5-Substituted Amino-[1,3,4]-Thiadiazoles, Gülgün Ayhan Kilcigi̇l, Canan Kuş, Nurten Altanlar, Süheyla Özbey
Synthesis And Antimicrobial Evaluation Of Some New 2-(2-(P-Chlorophenyl) Benzimidazol-1-Yl Methyl)-5-Substituted Amino-[1,3,4]-Thiadiazoles, Gülgün Ayhan Kilcigi̇l, Canan Kuş, Nurten Altanlar, Süheyla Özbey
Turkish Journal of Chemistry
Some 2-(2-(p-chlorophenyl)benzimidazol-1-ylmethyl)-5-substituted amino-[1,3,4]-thiadiazoles were synthesized and their in vitro antimicrobial activities were tested against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Candida albicans and Candida krusei. Compounds 1b and 12b which possess remarkable activity against C. albicans and marginal activity against C. krusei were found to be the most active compounds in this series. Single crystal X-ray diffraction analysis was performed for compound 8b.
Synthesis Of Mannich Bases Of Some 2,5-Disubstituted 4-Thiazolidinones And Evaluation Of Their Antimicrobial Activities, Handan Altintaş, Öznur Ateş, Seher Bi̇rteksöz, Gülten Ötük, Meltem Uzun, Di̇lek Şanata
Synthesis Of Mannich Bases Of Some 2,5-Disubstituted 4-Thiazolidinones And Evaluation Of Their Antimicrobial Activities, Handan Altintaş, Öznur Ateş, Seher Bi̇rteksöz, Gülten Ötük, Meltem Uzun, Di̇lek Şanata
Turkish Journal of Chemistry
4-Carbethoxymethyl-2-[(\alpha -chloropropionyl/\alpha -bromobutyryl/\alpha-chloro-(\alpha-phenyl)acetyl)amino]thiazoles (2a-c) were synthesized by the reaction of 4-carbethoxymethyl-2-aminothiazole (1) with \alpha-chloropropionyl chloride, \alpha-bromobutyryl bromide and \alpha-chloro-\alpha -phenylacetyl chloride, respectively, which were then refluxed with ammonium thiocyanate to obtain 5-substituted 2-[(4-carbethoxymethylthiazol-2-yl)imino]-4-thiazolidinones (3a-c). 3a-c were stirred with formaldehyde and various secondary amines to gain 15 novel compounds with the structure 5-substituted 5-(N,N-disubstituted aminomethyl)-2-[(4-carbethoxymethylthiazol-2-yl)imino]-4- thiazolidinones (4a-o). The antibacterial activities of the compounds against S. aureus ATCC 6538, S. epidermidis ATCC 12228, E. coli ATCC 8739, K. pneumoniae ATCC 4352, P. aeruginosa ATCC 1539, S. typhi, Sh. flexneri and Pr. mirabilis ATCC 14153 were tested using disk diffusion, while the antifungal …
Polyphenolic Compounds And Antimicrobial Activity Of Quercus Aucheri Leaves, Mahmut Koray Sakar, Di̇dem Şöhretoğlu, Meral Özalp, Meli̇ke Eki̇zoğlu, Sonia Piacente, Cosimo Pizza
Polyphenolic Compounds And Antimicrobial Activity Of Quercus Aucheri Leaves, Mahmut Koray Sakar, Di̇dem Şöhretoğlu, Meral Özalp, Meli̇ke Eki̇zoğlu, Sonia Piacente, Cosimo Pizza
Turkish Journal of Chemistry
Chromatographic studies (CC, VLC, MPLC, and PTLC) on ethyl acetate extract from the leaves of Quercus aucheri yielded 2 flavonoids (quercetin 3-O-\alpha-L-arabinopyranoside (1), quercetin 3-O-\beta-D-galactopyranoside (2)) and 2 tannin precursors and a procyanidin [(isolated as peracetates of (+)-catechin (3a), (+)-gallocatechin (4a) and epicatechin-(4\beta \to 8)-catechin (5a))]. The structures of the compounds were elucidated by UV, 1D-NMR (^1H, ^{13}C, TOCSY) and 2D-NMR (COSY, HSQC, HMBC) techniques. Different extracts (80% MeOH, EtOAc, n-BuOH and H_2O) from the leaves of Q. aucheri were investigated for their antimicrobial activity against 2 Gram-positive and 2 Gram-negative bacteria and 3 yeast-like fungi by a broth microdilution …
A New Approach Towards (\Pm)-4-Ipomeanol And Its 2-Furyl Regioisomer, Jurgen Krauss, Franz Bracher, Doris Unterreitmeier
A New Approach Towards (\Pm)-4-Ipomeanol And Its 2-Furyl Regioisomer, Jurgen Krauss, Franz Bracher, Doris Unterreitmeier
Turkish Journal of Chemistry
The cytotoxic furan derivative (\pm)-4-ipomeanol (1) and its regioisomer (8) were prepared in a new and efficient way starting from commercially available furan derivatives. In both cases the key step was a regioselective solvolysis of the terminal double bond with trifluoroacetic anhydride and boron trifluoride. The resulting compounds were tested in an agar diffusion assay against several bacteria and fungi, but did not show significant activity.