Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5276925 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Simply combining aryl boronic acids with 1,8-naphthyridine N-oxides and heating at 110 °C in toluene or dimethylformamide affords the corresponding 7-aryl-1,8-naphthyridines. The reaction is not sensitive to air or moisture and the process can be extended to other electron-deficient heteroaromatic N-oxides.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Linsey S. Bennie, Paul M. Burton, James A. Morris,