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The high-yield, stereoselective conversion of geraniol (3,7-dimethyl-trans -2,6-octadien-1-ol) to the insect juvenile hormone, methyl 12,14-dihomojuvenate (methylcis -10-epoxy-3,11-dimethyl-7-ethyl-trans, trans -2,6-tridecadienoate), has been performed by means of a nine-step route that avoids chromatography of intermediates.

Practical, Stereoselective Synthesis of Cecropia Juvenile Hormone