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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >A facile synthesis of alpha,alpha'-(EE)-bis(benzylidene)-cycloalkanones and their antitubercular evaluations.
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A facile synthesis of alpha,alpha'-(EE)-bis(benzylidene)-cycloalkanones and their antitubercular evaluations.

机译:α,α'-(EE)-双(亚苄基)-环烷酮的简便合成及其抗结核性评估。

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摘要

An economical and facile synthesis of alpha,alpha'-(EE)-bis(benzylidene)-cycloalkanones was achieved by the reaction of cycloalkanones with different aromatic aldehydes using ethanolic KOH in good yields. Few of the selected compounds were reduced with NaBH(4) to the respective alpha,alpha'-(EE)-bis(benzylidene)-cycloalkanols. All these compounds and our earlier synthesized cyclohexyl phenyl methanols were evaluated for their antitubercular, antifungal and antibacterial activities. Several compounds displayed moderate antitubercular activity with MIC=12.5-1.56 microg/mL. However, none of the compounds displayed any significant antifungal activity.
机译:通过使用乙醇KOH以高收率使环烷酮与不同的芳族醛反应,可以实现经济,便捷的α,α'-(EE)-双(亚苄基)-环烷酮合成。所选化合物很少用NaBH(4)还原为相应的α,α'-(EE)-双(亚苄基)-环烷醇。对所有这些化合物和我们较早合成的环己基苯基甲醇的抗结核,抗真菌和抗菌活性进行了评估。几种化合物显示中等的抗结核活性,MIC = 12.5-1.56 microg / mL。但是,没有一种化合物显示出任何显着的抗真菌活性。

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