Synthesis of functionalized naphthalenes, coumarines, quinolines, and isoflavones by chemo- and site-selective palladium-catalyzed coupling reactions Khaddour, Zien , 1984- Text theses Text Hochschulschrift 2015 2015 eng electronic resourceremoteComputermedienOnline-Ressourcetext/htmlapplication/pdfOnline-Ressource graph. Darst. I studied the site-selectivity of Suzuki cross-coupling reactions of the bis(triflate) of naphthoates, coumarines, and isoflavones. In addition, the chemo-selectivity of Suzuki cross-coupling reactions of naphthoates and quinolones containing bromide and triflate leaving groups were studied. In this context, were prepared various arylated pharmacologically relevant heterocycles which are not readily available by other synthetic methods. vorgelegt von M.Sc.Zien Khaddour Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2015 547.615 547.596 540 Organische Chemie 35.51 http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2015-0137-3 http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2015-0137-3&pdf http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2015-0137-3 Synthesis of functionalized naphthalenes, coumarines, quinolines, and isoflavones by chemo- and site-selective palladium-catalyzed coupling reactions--(DE-627)83182705X urn:nbn:de:gbv:28-diss2015-0137-3 oclc: 935899371 ppn: (DE-627)833029622