| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5261748 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
N-Arylidene-2-aryl-imidazo[1,2-a]azin-3-amines were synthesized via a one-pot, four-component condensation reaction using a 2-aminoazine, toluene-4-sulfonylmethyl isocyanide (TsCH2NC), and two equivalents of readily available aromatic aldehydes. The reaction was performed in diethyl ether as the solvent, with p-toluenesulfonic acid (p-TSA) as the catalyst at reflux temperature.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![A one-pot four-component synthesis of N-arylidene-2-aryl-imidazo[1,2-a]azin-3-amines](/preview/png/5261748.png "First Page Preview: A one-pot four-component synthesis of N-arylidene-2-aryl-imidazo[1,2-a]azin-3-amines")
Authors
Abbas Rahmati, Ali Moazzam, Zahra Khalesi,