603128-17-2Relevant academic research and scientific papers
Pd-catalyzed intramolecular direct arylations at high temperature
Franck, Philippe,Hostyn, Steven,Dajka-Halász, Beáta,Polonka-Bálint, ágnes,Monsieurs, Katrien,Mátyus, Peter,Maes, Bert U.W.
, p. 6030 - 6037 (2008/12/20)
Pd-catalyzed cyclodehydrohalogenation involving oxidative addition of aromatic C-Br or activated azaheteroaromatic C-Cl bonds and C(sp2)-H activation have been investigated at high reaction temperatures (180-200 °C). This allowed the fast (10-3
Synthesis of the dibenzo[f,h]phthalazine and dibenzo[f,h]cinnoline skeleton via a 'Suzuki-Pd-catalyzed intramolecular arylation' and a 'Suzuki-Pschorr' approach
Tapolcsányi, Pál,Maes, Bert U. W.,Monsieurs, Katrien,Lemière, Guy L. F.,Riedl, Zsuzsanna,Hajós, Gy?rgy,Van Den Driessche, Bart,Dommisse, Roger A.,Mátyus, Péter
, p. 5919 - 5926 (2007/10/03)
Palladium-catalyzed intramolecular arylation of 2-benzyl-5-(2-bromophenyl)-4-phenylpyridazin-3(2H)-one yielded hitherto unknown 2-benzyldibenzo[f,h]phthalazin-1(2H)-one. The synthesis of this new tetracyclic pyridazinone from 2-benzyl-5-(2-aminophenyl)-4-phenylpyridazin-3(2H)-one via a Pschorr type reaction was also investigated. Similarly, the construction of 2-methyldibenzo[f,h]cinnolin-3(2H)-one from 2-methyl-5-(2-bromophenyl)-6-phenylpyridazin-3(2H)-one and 2-methyl-5-(2-aminophenyl)-6-phenylpyridazin-3(2H)-one is also reported. Removal of the N-benzyl protective group of 2-benzyl-dibenzo[f,h]phthalazin-1(2H)-one with AlCl3 yielded unsubstituted dibenzo[f,h]phthalazin-1(2H)-one.
