Polysubstituted phenylisoxazoles were designed and synthesized to discover new antibacterial agents [3 + 2] cycloaddition. Thirty-five compounds with a phenylisoxazole scaffold were characterized by NMR, HRMS, and X-ray techniques. After being evaluated against (), (), and (), 4-nitro-3-phenylisoxazole derivatives were found to better antibacterial activities. Further studies have shown that the EC values of these compounds were much better than that of the positive control, bismerthiazol.
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http://dx.doi.org/10.1039/d2ra05009a | DOI Listing |
RSC Adv
September 2022
School of Pharmaceutical Sciences, Guizhou University Guiyang 550025 China
Polysubstituted phenylisoxazoles were designed and synthesized to discover new antibacterial agents [3 + 2] cycloaddition. Thirty-five compounds with a phenylisoxazole scaffold were characterized by NMR, HRMS, and X-ray techniques. After being evaluated against (), (), and (), 4-nitro-3-phenylisoxazole derivatives were found to better antibacterial activities.
View Article and Find Full Text PDFBeilstein J Org Chem
June 2010
Institut für Organische Chemie, Technische Universität Braunschweig, Postfach 3329, D-38023 Braunschweig, Germany.
A one-pot synthesis of 4-nitro-3-phenylisoxazole has been carried out by treatment of cinnamyl alcohol dissolved in acetic acid with sodium nitrite; in addition, 4-phenyl-3-furoxanmethanol was obtained in 40% yield.
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