1114775-86-8Relevant articles and documents
Efficient synthesis of novel six-member ring-fused quinoline derivatives via the Friedlaender reaction
Yang, Dingqiao,Guo, Wei,Cai, Yuepeng,Jiang, Lasheng,Jiang, Kailing,Wu, Xiaobing
, p. 229 - 233 (2008)
Novel quinolines fused with a six-member ring 5a-j were prepared in high yields (75-95%) via the Friedlaender reaction of dimethoxy-substituted o-aminobenzaldehydes of 3a or 3b with cyclic ketones 4, respectively. The structures of 5aj were determined by IR, 1H NMR, MS, and elemental analysis.