作者: Alexandr Shafir , Stephen L. Buchwald
DOI: 10.1021/JA063063B
关键词: Palladium 、 Organic chemistry 、 Molecule 、 Coupling reaction 、 Aryl 、 Chemistry 、 Catalysis 、 Polymer chemistry 、 Reaction rate 、 Amination 、 Copper
摘要: Through the use of cyclic beta-diketones as supporting ligands, copper-catalyzed coupling aryl iodides with aliphatic amines occurs at room temperature in little 1 h. These high reaction rates allow for a wide range and heteroaryl temperature. This method is highly tolerant number reactive functional groups, including -Br aromatic -NH2 well phenolic -OH. The selectivity CuI-beta-diketone catalyst represents useful complement to palladium-based methods.