Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 7, Issue 3, Pages 492-498Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9qo01334b
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Funding
- Youth Innovation and Technology Project of Shandong Province [2019KJC021]
- Natural Science Foundation of Shandong Province [ZR2018MB009]
- International Cooperation Project of Qinghai Province [2018-HZ-806]
- Qinghai Key Laboratory of Tibetan Medicine Research [2017-ZJ-Y11]
- National Natural Science Foundation of China [31900298, 21302109]
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A mild and facile visible-light-mediated strategy has been proposed for the synthesis of 3-acyl quinoxalin-2(1H)-ones through acridine red catalyzed aerobic oxidative decarboxylative acylation of alpha-oxo-carboxylic acids with quinoxalin-2(1H)-ones at room temperature in air. Various 3-acyl quinoxalin-2(1H)-ones could be efficiently obtained in good yields with excellent functional group compatibility.
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