作者: Liang Wang , Da-Gang Guo , Yan-Yan Wang , Chang-Zheng Zheng
DOI: 10.1039/C4RA11747F
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摘要: Efficient synthetic procedures for the preparation of aroyl hydrazones were developed by converting corresponding ethyl ester into hydrazides, followed a reaction with 4-hydroxy-3-methoxy-benzaldehyde. A series aromatic hydrazides and characterized elemental analysis, IR, 1H NMR, 13C NMR thermogravimetric analysis. The thermal gravity analysis showed that compounds 3a–3d stable below 228.23, 227.65, 118.97 179.51 °C, respectively. antimicrobial activity towards Staplylococcus aureus, Escherichia coli Pseudomonas aeruginosa. antibacterial experiments indicated had higher than hydrazides. presence hydroxyl group, as well number position groups, important further enhance activity.