| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5142866 | Chinese Chemical Letters | 2017 | 5 Pages |
Abstract
A series of quinolino[3,4-b]quinoxalin-6(5H)-ones have been synthesized using an Ugi/deprotection/cyclization (UDC) strategy, followed by a nucleophilic aromatic substitution reaction. This scaffold was thought to be a very important intermediate for building bioactive compounds.
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Chemistry
Chemistry (General)
Authors
Yong Li, Jie Lei, Jia Xu, Dian-Yong Tang, Zhong-Zhu Chen, Jin Zhu, Chuan Xu,