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- W1658902400 abstract "N-Aryl-3,4,5,6-tetrahydrophthalimides (I) and other two series of cyclic imide types of compounds (II & III) have been found active as pre-emergence or early post-emergence herbicides. The compounds showed activity at low rates on many grassy and broadleaf weeds and were exceptionally phytotoxic to hairy galinsoga, common purslane and toothcup. Futher biological and biochemical studies showed that these cyclic imide herbicides belonged to the category of diphenylether herbicides having 0-substituent(s) such as CNP or nitrofen in their mechanism of action. In the context of development of cyclic imide herbicides, an information has been obtained on the structural characteristics required for herbicidal activity and a hypothesis that the alkylene ring, the electrondonating moiety, the imide ring and p-substituted ary ring are the prerequisite for activity is presented." @default.
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- W1658902400 date "1979-01-01" @default.
- W1658902400 modified "2023-09-23" @default.
- W1658902400 title "Structure - Activity Relationship of Cyclic Imide Herbicides" @default.
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- W1658902400 doi "https://doi.org/10.1016/b978-0-08-022349-0.50036-9" @default.
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