The enantiospecific anti-phytopathogenic fungal activity of a new type of coumarin bearing a phenylpropanoid unit at the 3-position was found. (S)-3-[1-Methoxy-3-(4-methoxyphenyl)prop-2-yl]coumarin ((S)-5: EC50=16.5 µM) was 30 times more effective than the (R)-form against the Alternaria alternata Japanese pear pathotype. Derivatives bearing different substituents on the 7'-aromatic ring and the coumarin ring were synthesized to discover the more potent compounds. The 3'-CF3 and 4'-CF3 derivatives, 39 and 40, respectively, had the lowest EC50 values (1-2 µM) in this project, suggesting that the size of the electron-withdrawing and hydrophobic substituents at these positions gave an advantage. On the coumarin ring, the presence of the OCH3 or CH3 group at the 5-position accelerated the activity, as the (4'-OCH3, 5-OCH3) derivative 41 and (4'-OCH3, 5-CH3) derivative 45 were, respectively, 4-5 times more potent than the 4'-OCH3 derivative (S)-5.
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