Synthesis and insecticidal activity of lipophilic amides. Part 7. Alternative aromatic groups for phenyl in 6-phenylhexa-2,4-dienamides.

Autor: Elliott, Michael1, Farnham, Andrew W.1, Janes, Norman F.1, Johnson, Diana M.1, Pulman, David A.1
Předmět:
Zdroj: Pesticide Science. 1989, Vol. 26 Issue 2, p199-208. 10p.
Abstrakt: Synthesis of a wide range of analogues of the lead compound, N- 2-methylpropyl-6-phenylhexa-2,4-dienamide, in which phenyl was replaced by other aromatic systems is reported. In cases where rearrangement rendered the N- 2-methylpropyl compound less accessible, N-2,2-dimethylpropyl substitution was used, because rearrangement was then suppressed. Several of the groups examined, for instance 2-naphthyl, enhanced insecticidal activity, and when appropriately substituted, particularly with halogen, led to the most active compounds discovered in this series. [ABSTRACT FROM AUTHOR]
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