PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles
A metal-free promoted direct oxidative C–N bond coupling of quinoxalinones and azoles for the rapid and effective synthesis of potent pharmaceutical important 3-(azol-1-yl)quinoxalin-2-one has been developed. Employing PIDA as the easily available mediator, the desired coupling products were isolate...
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th-mahidol.762802022-08-04T18:23:04Z PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles Watchara Wimonsong Sirilata Yotphan Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics A metal-free promoted direct oxidative C–N bond coupling of quinoxalinones and azoles for the rapid and effective synthesis of potent pharmaceutical important 3-(azol-1-yl)quinoxalin-2-one has been developed. Employing PIDA as the easily available mediator, the desired coupling products were isolated in moderate to excellent yields with a good substrate scope under operational simplicity and mild reaction conditions. Preliminary mechanistic studies suggested that a radical process is likely to be involved in the reaction. 2022-08-04T08:12:00Z 2022-08-04T08:12:00Z 2021-02-12 Article Tetrahedron. Vol.81, (2021) 10.1016/j.tet.2020.131919 14645416 00404020 2-s2.0-85099636406 https://repository.li.mahidol.ac.th/handle/123456789/76280 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099636406&origin=inward |
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Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Watchara Wimonsong Sirilata Yotphan PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles |
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A metal-free promoted direct oxidative C–N bond coupling of quinoxalinones and azoles for the rapid and effective synthesis of potent pharmaceutical important 3-(azol-1-yl)quinoxalin-2-one has been developed. Employing PIDA as the easily available mediator, the desired coupling products were isolated in moderate to excellent yields with a good substrate scope under operational simplicity and mild reaction conditions. Preliminary mechanistic studies suggested that a radical process is likely to be involved in the reaction. |
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Mahidol University |
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Mahidol University Watchara Wimonsong Sirilata Yotphan |
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Article |
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Watchara Wimonsong Sirilata Yotphan |
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Watchara Wimonsong |
title |
PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles |
title_short |
PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles |
title_full |
PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles |
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PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles |
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PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles |
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pida-induced oxidative c–n bond coupling of quinoxalinones and azoles |
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2022 |
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https://repository.li.mahidol.ac.th/handle/123456789/76280 |
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