par Aksenov, Alexander A.V.;Rubin, Michael;Aksenov, Dmitrii D.A.;Orazova, Naila N.A.;Aksenov, Nicolai N.A.;Griaznov, Georgii G.D.;De Carvalho, Annelise;Kiss, Robert ;Mathieu, Véronique ;Kornienko, Alexander
Référence Journal of organic chemistry, 82, 6, page (3011-3018)
Publication Publié, 2017-03
Référence Journal of organic chemistry, 82, 6, page (3011-3018)
Publication Publié, 2017-03
Article révisé par les pairs
Résumé : | Indolo[3,2-c]quinolones have been efficiently synthesized via an acid-mediated, one-pot, three-component condensation of arylhydrazines, o-aminoacetophenones, and triazines or nitriles. The synthetic application of this method is showcased by the concise synthesis of isocryptolepine alkaloid and a series of its synthetic analogues with demonstrated cancer cell antiproliferative activities. |