The Mizoroki-Heck reaction is a palladium-catalyzed carbon–carbon bond forming process which is widely used in organic and organometallic synthesis. It has seen increasing use in the past decade as chemists look for strategies enabling the controlled construction of complex carbon skeletons.
The Mizoroki-Heck Reaction is the first dedicated volume on this important reaction, including topics on:
- mechanisms of the Mizoroki-Heck reaction
- intermolecular Mizoroki-Heck reactions
- focus on regioselectivity and product outcome in organic synthesis
- waste-minimized Mizoroki-Heck reactions
- intramolecular Mizoroki-Heck reactions
- formation of heterocycles
- chelation-controlled Mizoroki-Heck reactions
- the Mizoroki-Heck reaction in domino processes
- oxidative heck-type reactions (Fujiwara-Moritani reactions)
- Mizoroki-Heck reactions with metals other than palladium
- ligand design for intermolecular asymmetric Mizoroki-Heck reactions
- intramolecular enantioselective Mizoroki-Heck reactions
- desymmetrizing Mizoroki-Heck reactions
- applications in combinatorial and solid phase syntheses, and the development of modern solvent systems and reaction techniques
- the asymmetric intramolecular Mizoroki-Heck reaction in natural product total synthesis
Several chapters are devoted to asymmetric Heck reactions with particular focus on the construction of otherwise difficult-to-obtain sterically congested tertiary and quaternary carbons. Industrial and academic applications are highlighted in the final section. The Mizoroki-Heck Reaction will find a place on the bookshelves of any organic or organometallic chemist.
