3-(7'-Aryl-9'-hydroxyprop-8'-yl)coumarin, which is a structural isomer of a -2-hydroxybenzylidene-γ-butyrolactone-type lignan, was stereoselectively synthesized and subjected to plant growth regulation examination. ()-4'-Methoxyphenyl derivative showed stereospecific plant growth suppressive activity. The significance of the presence of hydroxy group at the 9'-position for the activity was clarified. The effect of the substituent at the 7'-aryl group was also shown. The 3'-methoxy, 4'-methoxy, and 4'-trifluoromethyl derivatives , , and led to the most significant growth suppression of Italian ryegrass roots. The 2'-methoxy derivative and 4'-methoxy derivative provided the most growth suppressive activity against lettuce shoots and roots, respectively.
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http://dx.doi.org/10.1021/acs.jafc.2c01926 | DOI Listing |
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