For the first time, nickel-catalyzed silyl-Heck reactions are reported. Using simple phosphine-supported nickel catalysts, direct activation of silyl triflates has been achieved. These results contrast earlier palladium-catalyzed systems, which require iodide additives to activate silyl-triflates. These nickel-based catalysts exhibit good functional group tolerance in the preparation of vinyl silanes, and unlike earlier systems, allows for the incorporation of trialkylsilanes larger than MeSi.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047519 | PMC |
http://dx.doi.org/10.1016/j.tet.2014.03.021 | DOI Listing |
Tetrahedron
July 2014
Department of Chemistry and Biochemistry, University of Delaware, Newark, DE, 19716.
For the first time, nickel-catalyzed silyl-Heck reactions are reported. Using simple phosphine-supported nickel catalysts, direct activation of silyl triflates has been achieved. These results contrast earlier palladium-catalyzed systems, which require iodide additives to activate silyl-triflates.
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