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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >New azoloazine derivatives as antimicrobial agents: Synthesis under microwave irradiations, structure elucidation, and antimicrobial activity
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New azoloazine derivatives as antimicrobial agents: Synthesis under microwave irradiations, structure elucidation, and antimicrobial activity

机译:新的唑唑嗪衍生物作为抗微生物剂:微波辐射下的合成,结构阐明和抗微生物活性

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摘要

With aiding of microwave radiation, new series of fused-thiazolopyrimidines and fused-triazolopyrimidines each with cycloheptane have been synthesized through the reaction of cycloheptane-thione with alpha-haloketones or hydrazonoyl chlorides in short-time intervals as well as high yield. Moreover, reaction of 2,7-bis(2-chlorobenzylidene)cycloheptan-1-one with o-aminothiophenol and heterocyclic amines afforded benzo[b]cyclohepta[e][1,4]thiazepine derivative and cycloheptapyrimidines fused with different azoles, respectively. The structure for all products was discussed and proved based on the results of spectral data and elemental analysis. Evaluation of the antimicrobial activity of selected products indicated that most of derivatives showed their potent activity exceeds the reference antibiotic in some cases.
机译:通过施加微波辐射,通过在短时间间隔和氢化氢氯酰氯的反应和高产率和高产率,通过将环庚烷或肼氯的反应合成了新的微波辐射。 此外,2,7-双(2-氯苄基)环庚烷-1-酮与o-氨基噻吩酚和杂环胺的反应得到苯并[b]环庚嗪[E] [1,4]噻嗪类衍生物和环庚嘧啶分别与不同的氮杂融合 。 讨论所有产品的结构,并根据光谱数据和元素分析的结果证明。 评价所选产品的抗微生物活性表明,大多数衍生物在某些情况下显示它们的效率超过参考抗生素。

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