Burns, Aaron C.2010-07-132010-07-132010-05https://hdl.handle.net/11299/91920University of Minnesota Ph.D. dissertation. May 2010. Major: Chemistry. Advisor: Thomas R. Hoye. 1 computer file (PDF); ix, 177 pages, appendix A.In the first portion of this work, an intramolecular Diels–Alder/Tsuji allylation assembly of functionalized trans-decalin systems will be discussed (Chapter I). This is presented in the context of synthetic studies toward the psychoactive (κ-opioid agonist) natural product salvinorin A. Synthetic studies of the sea lamprey (Petromyzon marinus) migratory pheromone will be discussed in Chapter II. In the third chapter, a structure activity relationship study of the sea lamprey migratory pheromone will be presented in which results suggest that the sea lamprey olfactory system is not uniquely and specifically recognizing the allo (i.e., 5α-H) configuration in bile acid derivatives.en-USBile acidIntramolecular Diels-AlderPheromoneSalvinorinSea lampreyTsuji allylationChemistryThesis or Dissertation