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Syntheses and biological activities of dihydro-5,6-dehydrokawain derivatives.
Tawata, S; Taira, S; Kobamoto, N; Ishihara, M; Toyama, S.
Affiliation
  • Tawata S; Department of Bioscience and Biotechnology, College of Agriculture, University of the Ryukyus, Okinawa, Japan.
Biosci Biotechnol Biochem ; 60(10): 1643-5, 1996 Oct.
Article in En | MEDLINE | ID: mdl-8987662
ABSTRACT
The syntheses and biological activities of dihydro-5,6-dehydrokawain derivatives against plant pathogenic fungi and termites were investigated. Dihydro-5,6-dehydrokawain was isolated by a simple method without chromatography from the leaves of Alpinia speciosa K. SCHUM. The white crystalline compound obtained was identified as dihydro-5,6-dehydrokawain (1) by instrumental analyses. 4-Hydroxy-6-(2-phenylethyl)-2H-pyran-2-one (3) was prepared by hydrolyzing dihydro-5,6-dehydrokawain. Three dihydro-5,6-dehydrokawain derivatives were synthesized by reacting 3 with phosphoric agents. Among the synthesized compounds, dimethyl [6-(2-phenylethyl)-2-oxo-2H-pyran-4-yl]phosphorothionate (4) had the strongest antifungal activity of 91% at 100 ppm against Corticium rolfsii.
Subject(s)
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Database: MEDLINE Therapeutic Methods and Therapies TCIM: Terapias_biologicas Main subject: Plants, Medicinal / Pyrones / Insecticides / Antifungal Agents Language: En Journal: Biosci Biotechnol Biochem Year: 1996 Type: Article Affiliation country: Japan
Search on Google
Database: MEDLINE Therapeutic Methods and Therapies TCIM: Terapias_biologicas Main subject: Plants, Medicinal / Pyrones / Insecticides / Antifungal Agents Language: En Journal: Biosci Biotechnol Biochem Year: 1996 Type: Article Affiliation country: Japan