| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10595478 | Bioorganic & Medicinal Chemistry Letters | 2013 | 18 Pages |
Abstract
Three-component coupling of aldehyde, 2-hydroxy-1,4-naphthoquinone and 3-amino-1,2,4-triazole has been achieved using a catalytic amount of sulfamic acid under solvent free conditions to produce a novel series of 6-aryl-benzo[h][1,2,4]-triazolo[5,1-b]quinazoline-7,8-dione derivatives in good yields and with high regioselectivity. These compounds are found to exhibit potent antitumoral properties.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Liqiang wu, Chong Zhang, Weilin Li,
![First Page Preview: Regioselective synthesis of 6-aryl-benzo[h][1,2,4]-triazolo[5,1-b]quinazoline-7,8-diones as potent antitumoral agents Regioselective synthesis of 6-aryl-benzo[h][1,2,4]-triazolo[5,1-b]quinazoline-7,8-diones as potent antitumoral agents](/preview/png/10595478.png)