| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5262949 | Tetrahedron Letters | 2013 | 4 Pages | 
Abstract
												α-Aminoamides are shown to be useful as ligands in Goldberg amidations. A number of α-aminoamides are examined and the importance of substitution on the α-aminoamides is explored. Acetamide is focused on as the nucleophilic coupling partner due to its low cost, stability and convenience as a protecting group. The initial substrate scope for these catalysts is explored and includes electronically activated and deactivated aryl bromides, however o-substituted aryl bromides are problematic.
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											Authors
												Aurpon W. Mitra, Marvin M. Hansen, Michael E. Laurila, Stanley P. Kolis, Joseph R. Martinelli, 
											