Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281878 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
A quick and efficient entry to 1,1-diarylethylenes via the reaction of polyoxygenated aryl N-tosylhydrazones with aryl triflates is described. The reaction employs the catalytic system Pd(OAc)2/XPhos, tBuOLi as the base and dioxane as the solvent. A variety of substituents on both the coupling partners' hydrazones and triflates are tolerated. This procedure provides a complementary route to the existing methods for the access to 1,1-diarylethylenes of biological interest.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bret Tréguier, Abdallah Hamze, Olivier Provot, Jean-Daniel Brion, Mouâd Alami,