4-Aryl and 4-vinyl quinolines were prepared via a sequential procedure involving regioselective Rh(acae)(C2H2)/dppf-catalyzed hydroarylation/hydrovinylation of beta-(2-aminophenyl)-alpha,beta-ynones with arylboronic acids or potassium aryl and vinyl trifluoroborates, followed by nucleophilic attack of the amino group onto the carbonyl.

Rh-Catalysed Sequential Hydroarylation/Hydrovinylation-Heterocyclization of beta-(2-Aminophenyl)-alpha,beta-ynones with Organoboron Derivatives: A New Approach to Functionalyzed Quinolines

ARCADI, Antonio;MARINELLI, Fabio
2006

Abstract

4-Aryl and 4-vinyl quinolines were prepared via a sequential procedure involving regioselective Rh(acae)(C2H2)/dppf-catalyzed hydroarylation/hydrovinylation of beta-(2-aminophenyl)-alpha,beta-ynones with arylboronic acids or potassium aryl and vinyl trifluoroborates, followed by nucleophilic attack of the amino group onto the carbonyl.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11697/12596
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