Department of Chemistry, Acadia University, Wolfville, NS, B4P 2R6, Canada.
Org Lett. 2013 Aug 16;15(16):4078-81. doi: 10.1021/ol4016354. Epub 2013 Jul 26.
A new strategy is reported for the synthesis of 6-aminoquinoline derivatives via a tandem Povarov reaction, dihydroquinoline oxidation, and imine reduction. These products allow access to symmetrical as well as unsymmetrical tetraarylpyrido[2,3-g]quinolines, potentially useful organic electronics.
报道了一种通过串联 Povarov 反应、二氢喹啉氧化和亚胺还原合成 6-氨基喹啉衍生物的新策略。这些产物可以得到对称和不对称的四芳基吡啶并[2,3-g]喹啉,它们可能是有用的有机电子材料。