Abstract
Abstract A popular synthetic target usually embodies unique structural features and/or implicates practical use. Chrysanthemic acid (1) which meets both criteria has indeed attracted enormous effort in its synthesis.1 From a utilitarian viewpoint, the total synthesis of trans-chrysanthemic acid is attended by the drawback of requiring optical resolution,2 because only the dextrorotatory antipode proves valuable for reconstitution of pyrethroid insecticides.
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