Successive replacement of halogen atoms in 4, 6-dihaloquinolines in cross-coupling reactions with arylboronic acids catalyzed by palladium and nickel complexes
IP Beletskaya, AV Tsvetkov, GV Latyshev…
文献索引：Beletskaya; Tsvetkov; Latyshev; Lukashev Russian Journal of Organic Chemistry, 2003 , vol. 39, # 11 p. 1660 - 1667
Abstract Conditions were found where in 6-halo-4-quinolines (halogen= iodine, bromine, or chlorine) the halogen atoms were replaced in succession by similar or different aryl groups in cross-coupling reactions with arylboric acids catalyzed by palladium and nickel complexes. Basing on successive Suzuki reaction a convenient procedure was developed for preparation of diarylquinolines that did not require isolation of the intermediate ...
