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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS, TRANSFORMATION OF 3-[(4-ARYLTHIAZOL-2-YL)-(p-TOLYL)AMINO]PROPANOIC ACIDS, BIS(THIAZOL-5-YL)PHENYL-, BIS(THIAZOL-5-YL)METHANE DERIVATIVES, AND THEIR ANTIMICROBIAL ACTIVITY
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SYNTHESIS, TRANSFORMATION OF 3-[(4-ARYLTHIAZOL-2-YL)-(p-TOLYL)AMINO]PROPANOIC ACIDS, BIS(THIAZOL-5-YL)PHENYL-, BIS(THIAZOL-5-YL)METHANE DERIVATIVES, AND THEIR ANTIMICROBIAL ACTIVITY

机译:合成,3 - [(4-芳基噻唑-2-基) - (对甲苯基)氨基]丙酸,双(噻唑-5-基)苯基 - ,双(噻唑-5-基)甲烷衍生物,和 他们的抗菌活性

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摘要

Bis(thiazol-5-yl)phenyl- and bis(thiazol-5-yl)methanes were synthesized by the reaction of 2,4-disubstituted thiazoles with aromatic aldehydes or formaldehyde. In addition, modification of the carboxyl group of the molecule was carried out. The reactions afforded compounds bearing various heterocyclic fragments. All the synthesized compounds were tested for their effect on Escherichia coli, Staphylococcus aureus and Mycobacterium luteum bacteria and Aspergillus niger and Candida tenuis fungi strains. Some of them exhibited antibacterial activity against test-culture Mycobacterium luteum.
机译:通过2,4-二取代的噻唑与芳香族醛或甲醛的反应合成双(噻唑-5-基)苯基和双(噻唑-5-基)甲烷。 另外,进行分子的羧基的改性。 反应得到了含有各种杂环片段的化合物。 测试所有合成的化合物对大肠杆菌,金黄色葡萄球菌和轻毛虫细菌和烟草菌和念珠菌和念珠菌真菌菌株的影响。 其中一些表现出针对试验培养的抗菌活性分枝杆菌。

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