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

✍ Scribed by Maddaford, Shawn P.; Keay, Brian A.

Book ID
111861372
Publisher
American Chemical Society
Year
1994
Tongue
English
Weight
342 KB
Volume
59
Category
Article
ISSN
0022-3263

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Scope and Limitations of the Palladium-C
Scope and Limitations of the Palladium-Catalyzed Cross-Coupling Reaction of in situ Generated Organoboranes with Aryl and Vinyl Halides
✍ Maddaford, Shawn P.; Keay, Brian A. πŸ“‚ Article πŸ“… 1994 πŸ› American Chemical Society 🌐 English βš– 342 KB

The in situ palladium(0)-catalyzed Suzuki reaction is shown to be an efficient method for the crosscoupling 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. In our previous a