1129563-62-7Relevant academic research and scientific papers
Diversity-oriented synthesis of functionalized 1-aminopyrroles by regioselective zinc chloride-catalyzed, one-pot 'conjugate addition/cyclization' reactions of 1,3-bis(silyl enol ethers) with 1,2-diaza-1,3-butadienes
Karapetyan, Vahuni,Mkrtchyan, Satenik,Schmidt, Andreas,Attanasi, Orazio A.,Favi, Gianfranco,Mantellini, Fabio,Villinger, Alexander,Fischer, Christine,Langer, Peter
, p. 1331 - 1336 (2008)
In a convenient one-pot process, the easily accessible 1,2-diaza-1,3- butadienes and 1,3-bis(silyl enol ethers) are converted into the previously unknown functionalized 1-aminopyrroles and 1-amino-4,5,6,7-tetrahydroindoles. The domino reaction proceeds through a zinc chloride-catalyzed Econjugate addition/cyclizationG sequence.
