Palladium catalyzed cross-coupling between phenyl- or naphthylboronic acids and benzylic bromides
作者:Sultan Chowdhury、Paris E. Georghiou
DOI:10.1016/s0040-4039(99)01566-x
日期:1999.10
The Suzuki-Miyaura palladium-catalyzed coupling reaction was extended to achieve mixed cross-coupling between substituted aryl and naphthyl mono- and bisbromomethanes with phenylboronic acid, 1-methoxy-2-naphthyl-, 3-methoxy-2-naphthyl-, or 4-methoxy-1-naphthylboronic acid to form the corresponding disubstituted methanes.
扩展了Suzuki-Miyaura钯催化的偶联反应,以实现取代的芳基和萘基单和双溴甲烷与苯基硼酸,1-甲氧基-2-萘基,3-甲氧基-2-萘基或4的混合交叉偶联。 -甲氧基-1-萘基硼酸形成相应的二取代甲烷。