Zim, DaniloGruber, Adriane S. [UNESP]Ebeling, GunterDupont, JairtonMonteiro, Adriano L.2014-05-272014-05-272000-09-07Organic Letters, v. 2, n. 18, p. 2881-2884, 2000.1523-7060http://hdl.handle.net/11449/66244Cyclopalladated compounds derived from the ortho-metalation of benzylic tert-butyl thioethers are excellent catalyst precursors for the Suzuki cross-coupling reaction of aryl bromides and chlorides with phenylboronic acid under mild reaction conditions. A broad range of substrates and functional groups are tolerated in this protocol, and highly catalytic activity is attained.2881-2884engSulfur-containing palladacycles: Efficient phosphine-free catalyst precursors for the Suzuki cross-coupling reaction at room temperatureArtigo10.1021/ol0063048Acesso restrito2-s2.0-0001292112