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(E)-2',3″-噻唑查尔酮的N-取代衍生物的合成及其抗菌性能

Synthesis and antimicrobial properties of N-substituted derivatives of (E)-2',3″-thiazachalcones.

作者信息

Usta Asu, Taşkıran Hacer

出版信息

Z Naturforsch C J Biosci. 2015;70(1-2):45-50. doi: 10.1515/znc-2014-4182.

Abstract

N-alkyl substituted 2',3″-thiazachalcones {3-[(1E)-3-(4-methylthiophene-2-yl)-3-oxoprop-1-en-1-yl]-1-alkyl (C5-12,14) pyridinium bromides} were synthesized by a two-step reaction. The newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR, elemental analysis and mass spectral studies. The synthesized compounds were tested for antibacterial activities and found to be more active against Gram-positive as compared to Gram-negative bacteria.

摘要

N-烷基取代的2',3″-噻唑查耳酮{3-[(1E)-3-(4-甲基噻吩-2-基)-3-氧代丙-1-烯-1-基]-1-烷基(C5-12,14)吡啶溴化物}通过两步反应合成。通过红外光谱、1H核磁共振、13C核磁共振、元素分析和质谱研究对新合成的化合物进行了表征。对合成的化合物进行了抗菌活性测试,发现它们对革兰氏阳性菌的活性比对革兰氏阴性菌的活性更强。

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