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- W4251711620 abstract "Zur Reaktion gebracht: Obwohl Estergruppen üblicherweise inert gegen Organopalladiumreagentien sind, gehen β-(2-Halogenanilino)ester eine intramolekulare Pd-katalysierte Acylierung zu Dihydrochinolin-4-onen ein (siehe Schema). Als Erklärung wird das intermediäre Auftreten eines viergliedrigen Azapalladacyclus postuliert, der die nucleophile Addition erleichtern soll." @default.
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- W4251711620 date "2007-09-24" @default.
- W4251711620 modified "2023-09-26" @default.
- W4251711620 title "Palladium-Catalyzed Intramolecular Nucleophilic Substitution at the Alkoxycarbonyl Group" @default.
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- W4251711620 doi "https://doi.org/10.1002/ange.200702176" @default.
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