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The Suzuki reaction uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide
The Suzuki Cross-Coupling reaction is the coupling of an aryl or vinyl boronic acid with an aryl or vinyl halide or triflate using a palladium catalyst.
Suzuki Reaction Mechanism
Watch our video to learn more about the Suzuki Reaction and its mechanisms.
Need reagents for the Suzuki Reaction?
Named Reactions eBook
History of the Suzuki Reaction
One of the best-known cross-coupling reactions is the Suzuki or Suzuki-Miyaura reaction, where organoboron compounds and organic halides or triflates react in the presence of a palladium catalyst to form carbon-carbon bonds. First reported in 1979, this reaction offers several advantages over other cross-coupling reactions, particularly the Stille reaction, boronic acids being much less toxic and environmentally damaging than the organostannanes.
Other Transition Metal-Catalyzed Couplings
Other Transition Metal-Catalyzed Couplings include:
For other types of reactions, visit our Named Reactions page.
Acroseal Packaging
Chemical reactions often involve the use of air- and moisture-sensitive solvents, and pyrophoric or hazardous reagents. Our AcroSeal packaging is a packaging solution designed to enable safe handling of these types of materials which are used in a variety of research and development applications, including NMR analysis and studies in drug discovery, agrochemicals, flavors and fragrances, and more.
Watch our video for more information.