| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279564 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
An efficient route to the biologically active naphthyl benzofuran derivative is described. The synthesis highlights a regioselective Suzuki coupling of a benzofuran and a dibromo substituted naphthalene. The scope of regioselective Suzuki coupling has been investigated.
Graphical abstractAn efficient route to the biologically active naphthyl benzofuran derivative is described. The synthesis highlights a regioselective Suzuki coupling of a benzofuran and a dibromo substituted naphthalene. The scope of regioselective Suzuki coupling has been investigated.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zheng Wang, Hassan Elokdah, Geraldine McFarlane, Sherry Pan, Madelene Antane,