Abstract
Esters selected from the combination of tricycloalkanecarboxylic acids and some representative pyrethroidal alcohols were prepared, and their insecticidal activities were measured by topical application on housefly, mosquito and German cockroach. Both the exo- and endo-isomers of 2,3-trimethylenenorbornane-2-carboxylic acid exhibited a high level of activity when esterified with m-phenoxymandelonitrile. Piperonyl butoxide showed a strong synergistic effect on some of the esters. Several structural resemblances were found among these active tricyclic acids and the chrysanthemummonocarboxylic acids, which were suggested to be related to insecticidal activity. © 1987 by the Agricultural Chemical Society of Japan.
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CITATION STYLE
Nakagawa, S., Takaishi, N., Inamoto, Y., Masuda, S., & Yamashita, O. (1987). Insecticidal tricycloalkanecarboxylic esters. Agricultural and Biological Chemistry, 51(5), 1355–1364. https://doi.org/10.1080/00021369.1987.10868225
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