کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
228727 | 464847 | 2015 | 6 صفحه PDF | دانلود رایگان |
Diverse 3,5,6,7-tetrahydrobenzofuran-4-one derivatives (3a–3n) were synthesized in high yields by ruthenium complex or rhodium complex catalyzed [3 + 2] cycloaddition. The antibacterial activities of these 3,5,6,7-tetrahydrobenzofuran-4-ones were evaluated against Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa, and Enterobacter aerogenes) and Gram-positive bacteria (Bacillus cereus and Staphylococcus aureus). In particular, compound 3b showed the highest antibacterial activity against P. aeruginosa and S. aureus (both MICs: 2 μg/mL). Compound 3l, which has the 2H-pyrano[2,3-b]benzofuran skeleton, exhibited excellent inhibitory activity against B. cereus (MIC: 0.5 μg/mL) as compared with ciprofloxacin (MIC: 2 μg/mL) and ampicillin (MIC: 1 μg/mL).
Figure optionsDownload as PowerPoint slide
Journal: Journal of Industrial and Engineering Chemistry - Volume 22, 25 February 2015, Pages 378–383