Synthesis and Biological Activity of Some Thiosemicarbazide

Rohit. R. Wakodkar, M. Farooqui, P. Kulkarni, D. D. Kayande
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Abstract

In this paper, thiosemicarbazone derivatives have been prepared from substituted aromatic aldehyde and thiosemicarbazide in presence of sodium chloride. This method is an efficient, mild, inexpensive, non-toxic and environment benign catalyst. This protocol includes the reaction followed by using sodium chloride to accelerate the reaction in aqueous ethanol. The structure of synthesized compounds were determined by IR, 1H NMR, 13C NMR and mass spectroscopies as well as the compounds were also screened for antibacterial and antifungal activity against certain Gram-negative and Gram-positive bacteria and fungal pathogens.
某些硫代氨基脲的合成及其生物活性研究
本文在氯化钠的存在下,以取代芳醛和硫代氨基脲为原料制备了硫代氨基脲衍生物。该方法是一种高效、温和、廉价、无毒、对环境无害的催化剂。该方案包括反应,然后使用氯化钠在乙醇水溶液中加速反应。通过IR、1H NMR、13C NMR和质谱对合成的化合物进行了结构鉴定,并对某些革兰氏阴性菌和革兰氏阳性菌及真菌病原体进行了抗菌和抗真菌活性筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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