929602-11-9Relevant academic research and scientific papers
Pd-catalyzed regioselective hydroarylation of α-(2-aminoaryl)-α,β-ynones with organoboron derivatives as a tool for the synthesis of quinolines: experimental evidence and quantum-chemical calculations
Arcadi, Antonio,Aschi, Massimiliano,Marinelli, Fabio,Verdecchia, Mirella
, p. 5354 - 5361 (2008/09/21)
The Pd-catalyzed hydroarylation of β-(2-aminoaryl)-α,β-ynones with organoboron derivatives, leading to 2,4-diarylquinolines in good to excellent yields through sequential cycloamination, has been investigated. The reaction is catalyzed by both Pd(II) and
Rh-catalyzed sequential hydroarylation/hydrovinylation-heterocyclization of β-(2-aminophenyl)-α,β-ynones with organoboron derivatives: A new approach to functionalized quinolines
Abbiati, Giorgio,Arcadi, Antonio,Marinelli, Fabio,Rossi, Elisabetta,Verdecchia, Mirella
, p. 3218 - 3224 (2008/09/17)
4-Aryl and 4-vinyl quinolines were prepared via a sequential procedure involving regioselective Rh(acac)(C2H2)/dppf-catalyzed hydroarylation/hydrovinylation of β-(2-aminophenyl)-α,β-ynones with arylboronic acids or potassium aryl and
