Syntheses and Biological Activities of Dihydro-5, 6-dehydrokawain Derivatives

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.