“…1). [16][17][18][19][20][21] Many of the classical methods, such as Ptzinger, Skraup, Friedlander, Doebner von Miller, Conrad-Limbach, and Combes reactions, known for the synthesis of quinolines are limited by harsh reaction conditions, limited substrate scope and low yields. 22 Among the various synthetic strategies, 23,24 Lewis acid promoted tandem cyclization reaction of N-aryl imines with terminal alkynes under oxidative condition allows access to a variety of 2,4-disubstituted quinolines.…”