| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266382 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Controlling the reaction temperature at 50 °C, 80 °C, and 110 °C, respectively, the iodine-catalyzed reaction of 2-aminobenzamides with 1,3-cyclohexanediones gave structurally diversified products. In the latter, it gave bis-quinazolin-4(3H)-ones unexpectedly, with 1,3-cyclohexanediones ring-opening.
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Authors
Lian Lu, Mei-Mei Zhang, Hong Jiang, Xiang-Shan Wang,