| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9564715 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
An efficient route to the preparation of 2-amino-3-hydroxy-4-substituted pyridines via regioselective metalation and subsequent alkylation of the [1,3]oxazolo[4,5-b]pyridin-2(3H)-one ring system is described.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis of 2-amino-3-hydroxy-4-substituted pyridines via regioselective metalation of 3-(1-ethylpropyl)-[1,3]oxazolo[4,5-b]pyridin-2(3H)-one and application to corticotropin releasing factor1 receptor ligands](/preview/png/9564715.png "First Page Preview: Synthesis of 2-amino-3-hydroxy-4-substituted pyridines via regioselective metalation of 3-(1-ethylpropyl)-[1,3]oxazolo[4,5-b]pyridin-2(3H)-one and application to corticotropin releasing factor1 receptor ligands")
Authors
Richard A. Hartz, Kausik K. Nanda, Charles L. Ingalls,