| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5278063 | Tetrahedron Letters | 2010 | 4 Pages | 
Abstract
												Mg-promoted reduction of benzophenones in the presence of ethyl trifluoroacetate and trimethylchlorosilane in N-methyl-2-pyrrolidinone afforded the corresponding cross-coupling products, which were easily transformed into C-trifluoroacetylated compounds of benzophenones through desilylation by tetrabutylammonium fluoride.
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											Authors
												Hirofumi Maekawa, Taro Ozaki, Ikuzo Nishiguchi, 
											