Dyotropic rearrangements of fused, tricyclic beta-lactones are described that proceed via unprecedented stereospecific, 1,2-acyl migrations delivering bridged, spiro-gamma-butyrolactones. A unique example of this dyotropic process involves a fused bis-lactone possessing both beta- and delta-lactone moieties which enabled rapid access to the core structures of curcumanolide A and curcumalactone. Our current mechanistic understanding of the latter dyotropic process, based on computational studies, is also described. Other key transformations in the described divergent syntheses of (-)-curcumanolide A and (-)-curcumalactone from a common intermediate (11 and 12 steps from 2-methyl-1,3-cyclopentanedione, respectively), include a catalytic, asymmetric nucleophile (Lewis base)-catalyzed aldol-lactonization (NCAL) leading to a tricyclic beta-lactone, a Baeyer-Villiger oxidation in the presence of a beta-lactone, and highly facial-selective and stereocomplementary reductions of an intermediate spirocyclic enoate. The described dyotropic rearrangements significantly alter the topology of the starting tricyclic beta-lactone, providing access to complex spirocyclic cyclopentyl-gamma-lactones and bis-gamma-lactones in a single synthetic operation.