Visible light promoted benzoylation of quinoxalinone-2(1<italic>H</italic>)-ones
Author:
Publisher
Science China Press., Co. Ltd.
Subject
Multidisciplinary
Link
https://engine.scichina.com/doi/pdf/26FA963BDEA14D2B9589875F777EE538
Reference36 articles.
1. Ramli Y, Moussaif A, Karrouchi K, et al. Pharmacological profile of quinoxalinone. J Chem, 2014, 2014: 1−21.
2. Willardsen J A, Dudley D A, Cody W L. Design, synthesis, and biological activity of potent and selective inhibitors of blood coagulation factor Xa. J Med Chem, 2004, 47: 4089-4099.
3. Piras S, Loriga M, Carta A. Novel 3-benzoyl-2-piperazinylquinoxaline derivatives as potential antitumor agents. J Heterocyclic Chem, 2006, 43: 541-548.
4. Cavazzuti A, Paglietti G, Hunter W N. Discovery of potent pteridine reductase inhibitors to guide antiparasite drug development. Proc Natl Acad Sci USA, 2008, 105: 1448-1453.
5. Cao H Y, Ma S S, Yao Y L. Synthesis of β-nitro ketone by visible light photoredox catalysis (in Chinese). Chin Sci Bull, 2022, 67: 2413-2422.
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