Scope and Limitations of the Palladium-Catalyzed Cross-Coupling Reaction of in Situ Generated Organoboranes with Aryl and Vinyl Halides

Article abstract of DOI:10.1021/jo00101a001

The in situ palladium(0)-catalyzed Suzuki reaction is shown to be an efficient method for the cross-coupling of aryl-, furyl-, primary, and benzylic boranes with aryl or vinyl bromides and iodides without the isolation of the organoboronic acid or the addition of any external base.