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Synthesis of highly functionalized carbacycles, heterocycles and silylium-arene adducts by cyclocondensations, palladium catalyzed cross-coupling reactions and activation by [Me3Si]+ cation ( Dissertationsschrift )

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The Me3SiOTf-mediated condensation of 1-ethoxy-2-fluoro-1,3-bis trimethylsilyloxy) 1,3-dienes with 3-cyanochromones afforded fluorinated azaxanthones or biaryls. The [4+2] cycloaddition of 1-ethoxy-2-fluoro-1,3-bis(trimethylsilyloxy)-1,3-diene with DMAD afforded dimethyl 4-fluoro-3,5-dihydroxyphthalate. Various arylated phthalates, naphthoates, indoles, are synthesized Pd(0)-catalyzed Suzuki cross-coupling reaction and studied. The experimental and theoretical study of the silylium arene adducts ([Me3Si-Ar][B(C6F5)4]) and the catalytic trimerisation of bissilylated diazomethane are studied.

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