Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267288 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
Palladium-catalyzed carbonylation of tosylates with phenyl formate is described. This procedure needs neither external carbon monoxide nor any pressure-resistant apparatus. A variety of cyclic and acyclic alkenyl tosylates can be converted into the corresponding phenyl esters in good yields. Furthermore, this method is effective for the one-pot synthesis of α,β-unsaturated amides.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tsuyoshi Ueda, Hideyuki Konishi, Kei Manabe,