Suzuki Reactions

Author:

Abstract

The Suzuki (also known as the Suzuki–Miyaura or Miyaura–Suzuki) coupling reaction, first reported in 1979, is probably one of the most important synthetic transformations developed in the 20th century for aryl–aryl bond formation. This chapter introduces the basics of Suzuki reactions before looking at the issues around these reactions and approaches towards greener processes, including choice of solvent and different catalytic approaches.

Publisher

The Royal Society of Chemistry

Reference45 articles.

1. Palladium-catalyzed cross-coupling reactions of organoboron compounds;Miyaura;Chem. Rev.,1995

2. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst

3. J.-E. Bäckvall, The Royal Swedish Academy of Sciences, Scientific Background on the Nobel Prize in Chemistry 2010, Palladium-catalyzed Cross Couplings in Organic Synthesis, 6 October 2010. https://www.nobelprize.org/uploads/2018/06/advanced-chemistryprize2010.pdf

4. Pd Metal Catalysts for Cross-Couplings and Related Reactions in the 21st Century: A Critical Review;Biffis;Chem. Rev.,2018

5. The Suzuki-Miyaura reaction after the Nobel prize;Beletskaya;Coord. Chem. Rev.,2019

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