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Synthesis and antimicrobial evaluation of diversely substituted spirooxindole derivatives

机译:螺取代异螺并吲哚衍生物的合成及抗菌性能评价

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A series of novel spirooxindole derivatives have been synthesized from isatin, malononitrile, and cyclic 1,3- dicarbonylcompounds through a highly efficient and green one-pot multicomponent reaction using tetrabutylammonium bromide (TBAB) as catalyst in ethanol under reflux condition. The synthesized compounds were evaluated for their antimicrobial activity. Antimicrobial studies showed that all the target compounds processing good antibacterial and antifungal activities.
机译:在乙醇中,在回流条件下,使用四丁基溴化铵(TBAB)作为催化剂,通过高效且绿色的一锅多组分反应,由靛红,丙二腈和环状1,3-二羰基化合物合成了一系列新颖的螺并吲哚衍生物。评价合成的化合物的抗微生物活性。抗菌研究表明,所有目标化合物均具有良好的抗菌和抗真菌活性。

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