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首页> 外文期刊>Chemistry Select >A Green and Efficient Protocol for the Synthesis of Phenylhydrazone Derivatives Catalyzed by Nanostructured Diphosphate Na2CaP2O7 and Screening of Their Antibacterial Activity
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A Green and Efficient Protocol for the Synthesis of Phenylhydrazone Derivatives Catalyzed by Nanostructured Diphosphate Na2CaP2O7 and Screening of Their Antibacterial Activity

机译:一种绿色和有效的方案,用于合成由纳米结构二磷酸盐NA2CAP2O7催化的苯基氢唑衍生物,并筛选其抗菌活性

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摘要

A new efficient strategy using diphosphate Na2CaP2O7 (DPH) for the synthesis of phenylhydrazone derivatives in solvent-free media is described. The synthesis of eight variously substituted phenylhydrazone derivatives (3a to 3h) can be carried out with a small amount of the catalyst, which can be easily recovered and reused several times without significant loss in catalytic activity. This protocol developed in our study is considered simple, clean, and characterized by short reaction time and high conversion. The antibacterial activity was evaluated for the synthesized compounds against Gram-positive and Gram- negative strains. A structure-activity relationship (SAR) study and the connection between antibacterial activity of the compounds was discussed and showed that electron donating groups increase the antibacterial activity.
机译:描述了使用二磷酸盐Na2CAP2O7(DPH)在无溶剂培养基中合成苯基氢唑衍生物的一种新的有效策略。 可以用少量催化剂进行八种不同取代的苯氢唑衍生物(3A至3H)的合成,可以轻松地恢复并重复几次,而不会在催化活性中显着损失。 在我们的研究中开发的该协议被认为是简单,清洁的,并且具有短反应时间和高转化率的特征。 评估了针对革兰氏阳性和革兰氏阴性菌株的合成化合物的抗菌活性。 讨论了化合物的抗菌活性之间的结构活性关系(SAR)研究,并表明电子捐赠组增加了抗菌活性。

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