Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267580 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
Triflic acid and triflimide were found to efficiently catalyze the formation of a wide diversity of diarylmethanes from the non-genotoxic benzylic acetates and electron-rich arenes or heteroarenes. The reaction worked best with acetates capable of generating a stabilized benzylic cationic species. In most cases, the reactions were conveniently run in the absence of solvent under mild conditions.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Oscar Mendoza, Guy Rossey, Léon Ghosez,