Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactions
- PMID: 20428032
- PMCID: PMC6257342
- DOI: 10.3390/molecules15042124
Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactions
Abstract
Since metal nanoparticles have a high surface-to-volume ratio and very active surface atoms, they are very attractive catalysts for a wide variety of organic and inorganic reactions, compared to bulk catalysts. Metal nanoparticles suspended in colloidal solutions and those adsorbed onto bulk supports have been used as catalysts for a wide variety of carbon-carbon bond formation reactions such as the Suzuki and Heck cross-coupling reactions. This review article highlights some of the latest advances in the application of noble metal nanoparticles as catalysts for these two industrially important classes of cross-coupling reactions. We will discuss several important advances in using metal nanocatalysts in Suzuki and Heck cross-coupling reactions such as investigations on the nanoparticle shape dependence on the catalytic activity, novel types of supported metal nanoparticles as nanocatalysts, and the use of bi-metallic, tri-metallic and multi-metallic nanoparticles as catalysts for the Suzuki and Heck cross-coupling reactions.
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References
-
- Miyaura N., Yanagi T., Suzuki A. The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases. Synth. Commun. 1981;11:513–519. doi: 10.1080/00397918108063618. - DOI
-
- Suzuki A. Synthetic Studies via the Cross-Coupling Reaction of Organoboron Derivatives with Organic Halides. Pure Appl. Chem. 1991;63:419–422. doi: 10.1351/pac199163030419. - DOI
-
- Miyaura N., Suzuki A. A Stereospecific Synthesis of Conjugated (E,Z)- and (Z,Z)-Alkadienes by a Palladium-Catalyzed Cross-Coupling Reaction of 1-Alkenylboranes with 1-Alkenyl Bromides. Tetrahedron Lett. 1981;22:127–130. doi: 10.1016/0040-4039(81)80166-9. - DOI
-
- Miyaura N., Yamada K., Suzuki A. A New Stereospecific Cross-Coupling by the Palladium-Catalyzed Reaction of 1-Alkenylboranes With 1-Alkenyl or 1-Alkynyl Halides. Tetrahedron Lett. 1979;20:3437–3440. doi: 10.1016/S0040-4039(01)95429-2. - DOI
-
- Miyaura N., Suzuki A. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds. Chem. Rev. 1995;95:2457–2483. doi: 10.1021/cr00039a007. - DOI
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