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Synthesis and in vitro antimicrobial studies of thiodihydropyrimidine derivatives
Journal of the Chinese Chemical Society ( IF 1.8 ) Pub Date : 2019-12-03 , DOI: 10.1002/jccs.201900197
Mani Pasupathi 1 , Namasivayam Santhi 1 , Kasi Venkatesan 2
Affiliation  

In the present study, a series of thiodihydropyrimidine derivatives were synthesized from different substituted aromatic aldehydes, ethyl acetoacetate, and urea/thiourea using a bimetallic TUD‐1 catalyst. The structures of all the synthesized compounds were characterized by melting point determination, thin layer chromatography (TLC), infrared (IR), 1HNMR, and 13C‐NMR values. All the synthesized compounds were screened for their antimicrobial activities against two gram positive bacteria, two‐gram negative bacteria, and two fungal strains.

中文翻译:

硫代二氢嘧啶衍生物的合成及体外抗菌研究

在本研究中,使用双金属TUD-1催化剂由不同的取代芳族醛,乙酰乙酸乙酯和尿素/硫脲合成了一系列硫代二氢嘧啶衍生物。所有合成化合物的结构均通过熔点测定,薄层色谱(TLC),红外(IR),1 HNMR和13 C-NMR值进行表征。筛选所有合成的化合物对两种革兰氏阳性细菌,两种革兰氏阴性细菌和两种真菌菌株的抗菌活性。
更新日期:2019-12-03
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