摘要
A novel rhodium-catalyzed oxidative [5 +1]annulation of 2-vinylanilines with alpha-diazocarbonyl compounds for the construction of quinoline-2-carboxylate derivatives has been developed. A series of functional groups such as methyl, methoxy, fluoro, chloro, bromo, cyano, and even thienyl substituents were tolerated well. This methodology has the potential for use in the pharmaceutical industry.
- 出版日期2018-1-11
- 单位江西师范大学