Abstract
Substituierte N- und O-Heterocyclen wurden durch Cycloisomerisierung von Dienen mithilfe eines Rutheniumcarben-Katalysators hergestellt. Die mit und ohne Trimethylsilyl(vinyl)ether erhaltenen Produkte sind unterschiedlich (siehe Schema, Cy=Cyclohexyl, Mes=2,4,6-Trimethylphenyl, Ts=para-Toluolsulfonyl).
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