Abstract
The dibromoalkenes (S)‐3 and (R)‐ and (S)‐4 are intermediates in the syntheses of the naturally occurring fungicidal butenolides fugomycin (1) and desoxyfugomycin (2), respectively. The stereoselective bromine–lithium exchange that leads to the carbenoid 12 and the vinyllithium reagent 17 a on the one hand, and palladium‐catalyzed coupling reactions of the dibromoalkene 3 and the bromolactone 22 on the other are key steps en route to the butenolides 1 and 2. The chiral building blocks (S)‐3, (R)‐4, and (S)‐4 are readily available from (R)‐isopropylideneglyceraldehyde 5, isobutyl (R)‐lactate 6 a, and ethyl (S)‐lactate 6 b, respectively. The synthetic procedure adopted here permits the absolute configuration of the natural products fugomycin (1) and desoxyfugomycin (2) to be assigned by comparison of their chiroptical properties with those of the synthetic products. The CD spectra of the bromolactone 22, calculated by two different density functional methods (TDDFT, DFT/MRCI), are found to be in good agreement with the measured spectra. On the basis of these calculations, the two CD bands observed could be assigned to n–π* and π–π* transitions, respectively. Fugomycin (1) and the synthetic butenolide 20 displayed high fungicidal activity against botrytis in greenhouse experiments, whereas the saturated lactone 21 was practically inactive.