By H. Geissbühler, P. C. Kearney and G. T. Brooks (Eds.)
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Extra info for Advances in Pesticide Science: Abstract and Addendum
Previous work in our laboratories has shown that carbamates derived from hydroxyindolines and hydroxy-3-H-indoles are insecticidal1. By regarding the hydroxyindoline system as a cyclised o-dialkylaminophenol a further series of carbamates can be envisaged. A search of the literature showed, to our surprise, that although carbamates containing the dialkylamino group are well known as acetylcholinesterase inhibitors2 and have been mentioned as insecticides, the combination of this group uith other substituents has rarely been described.
C. S. Perkin Trans 2, 1973, 1719 T. Nishimura and Y. Miyamoto Ι-9Π7 School of Hygienic Sciences, Kitasato University, Sagamihara-shi, Japan K. Matsumoto and T. , Yokohama-shi, Japan SYNTHESIS OF THIOSEMICARBAZONES OF 3-OXO-ESTERS AND AMIDES AND l-THIOCARBAMOYL-PYRAZOLINE-5-ONES AND THEIR ANTIFUNGAL ACTIVITY AGAINST PIRICULARIA ORYZAE. The purpose of this work is to synthesize the title compounds in order to know the structure-activity relationship and to find effective compounds to control blast of rice.
Et al, Computers & Chem, _1, 187 (1977) 2. T. Matsuo, et al, Agr. Biol. Chem. 40, (1) 247 (1976) G. Holan. F. O'Keefe, K. Rihs, R. T. Virgona CSIRO, Division of Applied Organic Chemistry, Melbourne, Victoria, Australia. NEW INSECTICIDES. STRUCTURES II-7 COMBINED DDT - ISOSTERES AND PYRETHROID The size limitation and the biological role of our previously postulated structural model for DDT-type of insecticides was used to design an insecticide 2,2-dimethyl1,1-bis (4-ethoxyphenyl)-cyclopropane, which is isosteric with DDT but also contains the dimethylcyclopropane part structure of pyrethroids.
Advances in Pesticide Science: Abstract and Addendum by H. Geissbühler, P. C. Kearney and G. T. Brooks (Eds.)