83297-64-7Relevant academic research and scientific papers
Synthesis of 1,11-dihydro-2H-[1,3]oxazolo[4′,5′:5,6]indeno[1,2- b]quinolin-2-ones with potential topoisomerase I inhibitory activity
Delot, Marc,Carato, Pascal,Furman, Christophe,Lemoine, Amelie,Lebegue, Nicolas,Berthelot, Pascal,Yous, Said
scheme or table, p. 3819 - 3822 (2010/03/03)
A series of 1,11-dihydro-2,11-[1,3]oxazolo[4′,5′:5,6]indeno[1, 2-b]quinolin-2-ones were prepared by means of Friedlaender condensations. The starting materials for the preparations were commercial substituted-2- aminoacetophenones and various 5,6-dihydro-2H-indeno[5,6-d][l,3]oxazole-2,7(3H)- diones that were synthesized from 2(3H)-benzoxazolones or their N-methyl analogues. Thieme Verlag Stuttgart.
Synthesis of 3-methyl-7-[2-(dimethylaminoethyl)oximino]-5-arylcyclopenta[f]benzoxaz olinones, potential ligands of the 5HT(1D) receptors
Varlet, Didier,Depreux, Patrick,Lesieur, Isabelle,Pfeiffer, Bruno
, p. 4319 - 4328 (2007/10/03)
The synthesis of 3-methyl-7-[2-(dimethylaminoethyl)oximino]-5-arylcyclopenta[f]benzoxaz olinones, potential ligands of the 5HT(1D) receptors is described through a 4 step reaction strategy from 3-methyl-6-acetyl benzoxazolinone.
