| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1257329 | Chinese Chemical Letters | 2015 | 4 Pages |
Abstract
A novel method for achieving a copper(II)-catalyzed domino reaction for the construction of 2-aryl quinazolinones, without the addition of any ligand and additive, has been developed. The domino reaction achieved N-(α-substituted)benzylation, benzylic CH amidation, and CC (or CH) bond cleavage.
Graphical abstractA novel method for achieving a copper(II)-catalyzed domino reaction for the construction of 2-aryl quinazolinones, without the addition of any ligand and additive, has been developed. The domino reaction achieved N-(α-substituted)benzylation, benzylic CH amidation, and carbon–carbon (or carbon–hydrogen) bond cleavage.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Ben-Quan Hu, Li-Xia Wang, Jun-Feng Xiang, Luo Yang, Ya-Lin Tang,