861843-76-7Relevant academic research and scientific papers
Chemoselective arylamination of β-bromovinylaldehydes followed by acid catalyzed cyclization: a general method for polycyclic quinolines
Some, Surajit,Ray, Jayanta K.
, p. 5013 - 5016 (2007)
A synthesis of polycyclic quinolines is described via palladium-catalyzed chemoselective arylamination of β-bromovinylaldehydes with aromatic amines followed by acid catalyzed cyclization.
Synthesis of 5,6-dihydrobenz[c]acridines: a comparative study
Karthikeyan,Meena Rani,Saiganesh,Balasubramanian,Kabilan
experimental part, p. 811 - 821 (2009/04/07)
5,6-Dihydrobenz[c]acridines were synthesized by the reaction of 1-chloro-3,4-dihydro-2-naphthaldehyde with aromatic amines under three different conditions:a.Thermolysis of 1-chlorovinyl-(N-aryl)imines prepared from 1-chloro-3,4-dihydro-2-naphthaldehyde.b
Selective palladium-catalyzed amination of β-chloroacroleins by substituted anilines
Hesse, Stéphanie,Kirsch, Gilbert
, p. 6534 - 6539 (2007/10/03)
β-Chloroacroleins can undergo a selective amination on their chloro position under palladium catalysis; in those conditions, no imine formation was observed. Their coupling with anilines carrying electron-donating or electron-withdrawing substituents proceeds in moderate to good yields and steric hindrance does not seem to be a limitation as o-substituted anilines react readily.
