期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 87, 期 11, 页码 7405-7413出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c00643
关键词
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资金
- Japan Society for the Promotion of Science (JSPS) [20K05510, 20H04819, 20H02779, 18H04650]
- Asahi Glass Foundation
- Grants-in-Aid for Scientific Research [20H02779, 20H04819, 20K05510] Funding Source: KAKEN
Visible-light-induced decarboxylative and deboronative reactions were achieved using two-molecule organic photoredox catalysts. The high solubility improved reaction efficiency and product yield. The oxidation potential of the electron-donor molecule can be tuned for a wide range of substrates.
Visible-light-induced decarboxylative and deboronative reactions using two-molecule organic photoredox catalysts, namely, phenanthrene (Phen) and biphenyl (BP), as electron donors and 9-cyano-10-methoxycarbonylanthracene1aas an electron acceptor were achieved. The high solubility of1asignificantly improved the reaction efficiency and product yield.In addition, the facile tuning of the oxidation potential of theelectron-donor molecule via the replacement of Phen with BPenabled the application of the two-molecule photoredox system toa wide range of substrates.
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