An intermolecular palladium-catalyzed diamination of unactivated alkenes
Á. Iglesias, E. G. Pérez, K. Muñiz
Angew. Chem. Int. Ed. 2010, 49, 8109-8111
Abstract: Palladium catalysis introduces two nitrogen groups in a new regio and chemoselective diamination of non-activated alkenes that proceeds under entirely intermolecular reaction control. This palladium-catalyzed reaction employs commercial nitrogen sources in combination with a hypervalent iodo(III) reagent as oxidant (see scheme; Tos = toluenesulfonyl).