Pyrethrone

Fujitani [6] separated the insecticidally active syrupy ester from pyrethrum flowers in 1909 and named the ester pyrethron. Yamamoto [7, 8] subjected the hydrolysis product of this pyrethron to ozone oxidation, and isolated Iram-caronic acid and aldehyde (1 and 2, respectively, Fig. 3). Although Yamamoto did not determine the structure of this acid, he presumed it to be pyrethron acid (Fig. 3). Eventually, the presence of a cyclopropane ring in the molecule of natural pyrethrins became clear for the first time in 1923. [Pg.6]

Yamamoto R (1923) The insecticidal principle in Chrysanthemum cinerariaefolium. Parts II and III. On the constitution of pyrethronic acid. J Chem Soc Jpn 44 311-330... [Pg.28]

Staudinger H, Ruzicka L (1924) Konstitution des Tetrahydro-pyrethrons. Insektentotende... [Pg.80]

Staudinger H, Ruzicka L (1924) Insektentotende Stoffe V. Synthese des Tetrahydro-pyrethrons, des Reduktionsproduktes des Pyrethrolons. Helv Chim Acta 7 245-259... [Pg.80]

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