Publication:
PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles

dc.contributor.authorWatchara Wimonsongen_US
dc.contributor.authorSirilata Yotphanen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2022-08-04T08:12:00Z
dc.date.available2022-08-04T08:12:00Z
dc.date.issued2021-02-12en_US
dc.description.abstractA 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.en_US
dc.identifier.citationTetrahedron. Vol.81, (2021)en_US
dc.identifier.doi10.1016/j.tet.2020.131919en_US
dc.identifier.issn14645416en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-85099636406en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/76280
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099636406&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titlePIDA-induced oxidative C–N bond coupling of quinoxalinones and azolesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099636406&origin=inwarden_US

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