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- Title
Catalysts for Suzuki–Miyaura Coupling Reaction.
- Authors
Len, Christophe
- Abstract
Among the main reactions in organic chemistry, the Suzuki-Miyaura cross-coupling reaction catalyzed by a homogeneous or heterogeneous palladium complex is undoubtedly the most important. Different titanium-dioxide-supported palladium catalysts are produced and characterized for a ligand-free Suzuki-Miyaura cross-coupling reaction [[6]]. Among these catalysts, Pd/TiO SB 2 sb (anatase-type) obtained by acetonitrile solution impregnation between palladium acetate and anatase-type TiO SB 2 sb demonstrates the best catalytic activity. The synthesis of a periodic mesoporous organosilica (PMO) structure functionalized with bipyridinium ionic liquid supported palladium (Pd@Bipy-PMO, 0.2 mol%) is reported and the hybrid catalysts are fully characterized [[8]].
- Subjects
SUZUKI reaction; ARYL chlorides; FLOW chemistry; CATALYSTS; PALLADIUM catalysts; CHEMICAL reactions
- Publication
Catalysts (2073-4344), 2020, Vol 10, Issue 1, p50
- ISSN
2073-4344
- Publication type
Editorial
- DOI
10.3390/catal10010050