Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5216324 | Tetrahedron | 2014 | 7 Pages |
Abstract
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 Me3Si.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jesse R. McAtee, Sara E.S. Martin, Andrew P. Cinderella, William B. Reid, Keywan A. Johnson, Donald A. Watson,