| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5272222 | Tetrahedron Letters | 2010 | 5 Pages | 
Abstract
												Trialkylsilyl triflimides generated in situ are unique catalysts for the electrophilic benzylation or allylation of trialkylsilylenol ethers or allyl trialkylsilanes with non-genotoxic alkylating reagents such as benzyl and allyl acetates. In most cases the reactions are fast at room temperature and yields are high. The reaction works particularly well with electron-rich benzyl donors including derivatives of pyrrole, indole and furane.
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											Authors
												Oscar Mendoza, Guy Rossey, Léon Ghosez, 
											