| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275124 | Tetrahedron Letters | 2007 | 4 Pages |
A systematic study of α-iodination and subsequent Suzuki-Miyaura couplings between non-attenuated enaminones and a wide range of aromatic boronic acids is reported. The microwave-assisted variant of this transformation furnished the α-arylenaminones in significantly shorter reaction times and slightly improved yields as compared to conventional heating.
Graphical abstractA systematic study of α-iodination and subsequent Suzuki-Miyaura couplings between non-attenuated enaminones and a wide range of aromatic boronic acids is reported. The microwave-assisted variant of this transformation furnished the products in significantly shorter reaction times and in slightly improved yields as compared to conventional heating.Download full-size image
