Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281245 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
1H-Quinazoline-2,4-diones were efficiently synthesized by selenium-catalyzed carbonylation of o-nitrobenzamides under relatively mild conditions. In situ-generated carbonyl selenide (SeCO) is proposed to initiate the catalytic carbonylation. Thus, a concise transition metal and phosgene-free synthetic route to potentially bioactive-substituted 1H-quinazoline-2,4-dione derivatives has been developed.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xiaowei Wu, Zhengkun Yu,