Abstract
The 6 S,7 S,10 R-, 6 S,7 S,10 S-, 6 R,7 R,10 S-, and 6 R,7 R,10 R-stereoisomers of the juvenile hormone III bisepoxide from higher Dipteran insects have been synthesised in high stereoisomeric purity. The route involves Sharpless epoxidation of geraniol to enantiomeric epoxyalcohols, which are each elaborated via separable diastereomeric bromohydrins.
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