1073950-83-0Relevant articles and documents
Regioselective synthesis of N-aminoisoindolones and mono-N- and di-N,N′-substituted phthalazones utilizing hydrazine nucleophiles in a palladium-catalyzed three-component cascade process
Grigg, Ronald,Sridharan, Visuvanathar,Shah, Mufakhrul,Mutton, Simon,Kilner, Colin,MacPherson, David,Milner, Peter
supporting information; experimental part, p. 8352 - 8356 (2009/04/11)
(Chemical Equation Presented) A palladium-catalyzed three-component cascade process for the synthesis of isoindolone and phthalazone derivatives is reported. The cascade process involves carbonylation of an aryl iodide/Michael acceptor to give an acylpalladium species which is intercepted by a hydrazine nucleophile. Intramolecular Michael addition follows to give either N-aminoisoindolones or mono-N- and di-N,N′-phthalazones depending on whether a monosubstituted or 1,2-disubstituted hydrazine nucleophile is used.