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Palladium-Catalyzed Alkoxycarbonylation Reactions of (e)-2 Carbonates
(Izmir Institute of Technology, 2013) Karagöz, Ezgi Şule; Artok, Levent; Artok, Levent; 04.01. Department of Chemistry; 04. Faculty of Science; 01. Izmir Institute of Technology
Transition metal-catalyzed carbon-carbon bond formation reactions are well-rounded methods to synthetic organic chemistry. One type of these reactions is the alkoxycarbonylation reactions performed in the presence of a transition metal catalyst, an alcohol and carbon monoxide atmosphere. Investigations on palladium-catalyzed alkoxycarbonylation reaction of allylic compounds leading to Î²,Î³-unsaturated esters have been performed. Moreover propargyl derivatives are prominent reactants for palladium-catalyzed alkoxycarbonylation reactions to yield allene esters which proceed through a Ïƒ-allenylpalladium intermediate. Palladium-catalyzed alkoxycarbonylation reaction of some enantio-enriched propargylic derivatives that facilitate unique centre-to-axis chirality transfer is still inadequate and essential. In this study, the palladium-catalyzed alkoxycarbonylation reaction of E-configured 2,4-enyne carbonates which afforded exclusively ester functionalized (E)-configured vinylallenes through the formation of Ïƒ-vinylallenylpalladium species was performed. Moreover the chirality transfer of the proposed method was also surveyed over an enantio-enriched E-enyne carbonate.

Master Degree / Yüksek Lisans Tezleri