Photoinduced Dehydrogenative Amination of Quinoxalin-2(1H)-ones with Air as an Oxidant
Author:
Affiliation:
1. State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, Tianjin 300071, People’s Republic of China
Funder
Nankai University
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02781
Reference85 articles.
1. Recent advances in the direct functionalization of quinoxalin-2(1H)-ones
2. Visible-light-induced three-component reaction of quinoxalin-2(1H)-ones, alkenes and CF3SO2Na leading to 3-trifluoroalkylated quinoxalin-2(1H)-ones
3. Transition-Metal-Free Direct C–H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature
4. Transition Metal-Free Iodosobenzene-Promoted Direct Oxidative 3-Arylation of Quinoxalin-2(H)-ones with Arylhydrazines
5. Transition Metal-Free Direct C-3 Arylation of Quinoxalin-2(1H )-ones with Arylamines under Mild Conditions
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1. Visible‐Light Mediated C‐3 Amination of Quinoxalin‐ 2(1H)‐ones via Electron Donor‐Acceptor Complexation;Asian Journal of Organic Chemistry;2024-07-06
2. Organophotoelectrocatalytic C(sp2)–H alkylation of heteroarenes with unactivated C(sp3)–H compounds;Chemical Communications;2024
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