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J Agric Food Chem ; 70(28): 8767-8775, 2022 Jul 20.
Article in English | MEDLINE | ID: mdl-35796683

ABSTRACT

3-(7'-Aryl-9'-hydroxyprop-8'-yl)coumarin, which is a structural isomer of a Z-2-hydroxybenzylidene-γ-butyrolactone-type lignan, was stereoselectively synthesized and subjected to plant growth regulation examination. (R)-4'-Methoxyphenyl derivative 3 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 10, 3, and 22 led to the most significant growth suppression of Italian ryegrass roots. The 2'-methoxy derivative 9 and 4'-methoxy derivative 3 provided the most growth suppressive activity against lettuce shoots and roots, respectively.


Subject(s)
Lignans , 4-Butyrolactone/pharmacology , Coumarins/pharmacology , Lactuca , Lignans/chemistry , Lignans/pharmacology , Plant Development
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