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Chrysanthemic acid is an organic compound that is related to a variety of natural and synthetic insecticides. It is related to the pyrethrin I and II, as well as the pyrethroids. One of the four stereoisomers, (1''R'',3''R'')- or (+)-''trans''-chrysanthemic acid (pictured), is the acid part of the ester pyrethrin I, which occurs naturally in the seed cases of ''Chrysanthemum cinerariaefolium''. Many synthetic pyrethroids, for example the allethrins, are esters of all four stereoisomers. Hermann Staudinger, Staudinger and Leopold_Ružička, Ružička named chrysanthemic acid in 1924.H. Staudinger, L. Ružička: "Insektentotende Stoffe H. Zur Konstitution der Chrysanthemummonocarbonsiiure und -dicarbonsiiure", Helv. Chem. Acta 7 (1924) 201
Many pyrethroids are accessible by re-esterification of chrysanthemic acid ethylester.
Biosynthesis
Chrysanthemic acid is derived from its pyrophosphate ester, which in turn is biosynthesis, produced naturally from two molecules of dimethylallyl diphosphate.
Industrial synthesis
Chrysanthemic acid is produced industrially in a cyclopropanation reaction of a diene as a mixture of trans isomer, cis- and trans isomers, followed by hydrolysis of the ester:
Many pyrethroids are accessible by re-esterification of chrysanthemic acid ethylester.
References
{{Insecticides Monoterpenes Cyclopropanes Carboxylic acids