| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5284919 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A regioselective 1,3-dipolar cycloaddition reaction between a nitrile imine and an enamine is described for the preparation of celecoxib. Nitrile imines are generated in situ from the corresponding hydrazonoyl benzenesulfonates.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lynette M. Oh,