1,1'-Methylene-3,3'-bis[(N-(tert-butyl)imidazol-2-ylidene] and Its Effect in Palladium-Catalyzed C-C Coupling
Shirin Nadri, Ezzat Rafiee, Sirous Jamali, Mohammad Joshaghani*
*Faculty of Chemistry, Razi University, Kermanshah 67149, Iran, Email: mjoshaghanirazi.ac.ir
S. Nadri, E. Rafiee, S. Jamali, M. Joshaghani, Synlett, 2015, 26, 619-624.
DOI: 10.1055/s-0034-1379954 (free Supporting Information)
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A catalytic system utilizing a chelate carbene ligand containing bulk tert-butyl groups has been used for palladium-catalyzed Heck and Suzuki coupling reactions. The catalyst system performs well with low loadings of Pd(OAc)2. Heck reactions with monosubstituted olefins provide the trans-configured products, while 1,1-disubstituted olefins favor the terminal product.
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palladium, carbene Ligand, C-C coupling, Heck reaction, Suzuki reaction