3-Phenyl-5-methyl-2H, 5H-furan-2-ones: tuning antifungal activity by varying substituents on the phenyl ring
…, V Balšánek, J Kuneš, V Buchta, K Waisser
Index: Pour, Milan; Spulak, Marcel; Balsanek, Vojtech; Kunes, Jiri; Buchta, Vladimir; Waisser, Karel Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 16 p. 1893 - 1895
Full Text: HTML
Citation Number: 38
Abstract
A series of racemic 3-phenyl-5-methyl-2H, 5H-furan-2-ones related to a natural product,(−) incrustoporine, was synthesized, and their antifungal activity evaluated. The key structural feature, furanone ring, was closed via H2SO4-mediated cyclization of 2-phenylpent-4-enoic acids. The compounds displayed antifungal activity, especially against filamentous fungi. Expressed as the minimum inhibition concentration (MIC) in μmol/L, the activity of the most ...
Related Articles:
[Miura; Okajima; Hondo; Nakagawa; Takahashi; Hosomi Journal of the American Chemical Society, 2000 , vol. 122, # 46 p. 11348 - 11357]
[Lai, Ping-Shan; Dubland, Joshua A.; Sarwar, Mohammed G.; Chudzinski, Michael G.; Taylor, Mark S. Tetrahedron, 2011 , vol. 67, # 39 p. 7586 - 7592]
[Tsuji, Jiro; Shimizu, Isao; Minami, Ichiro; Ohashi, Yukihiro; Sugiura, Teruo; Takahashi, Kazuhiko Journal of Organic Chemistry, 1985 , vol. 50, # 9 p. 1523 - 1529]
[Nawghare, Beena R.; Lokhande, Pradeep D. Synthetic Communications, 2013 , vol. 43, # 14 p. 1955 - 1963]
[Tsuji, Jiro; Takahashi, Kazuhiro; Minami, Ichiro; Shimizu, Isao Tetrahedron Letters, 1984 , vol. 25, # 42 p. 4783 - 4786]