Publication: Persulfate-promoted oxidative C-N bond coupling of quinoxalinones and: NH -sulfoximines
dc.contributor.author | Ladawan Sumunnee | en_US |
dc.contributor.author | Chaleena Pimpasri | en_US |
dc.contributor.author | Medena Noikham | en_US |
dc.contributor.author | Sirilata Yotphan | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2019-08-23T10:38:39Z | |
dc.date.available | 2019-08-23T10:38:39Z | |
dc.date.issued | 2018-01-01 | en_US |
dc.description.abstract | © The Royal Society of Chemistry. The persulfate-meditated oxidative C-N bond coupling of the C-H bond of quinoxalinones and the N-H bond of NH-sulfoximines is reported. The reaction proceeds smoothly under transition metal-free conditions and provides good to excellent yields of sulfoximidoyl-functionalized quinoxalinone products under mild conditions. The optimized conditions were found to be suitable for a range of sulfoximine and quinoxalinone substrates. This reaction offers a new and convenient strategy to directly install the sulfoximine moiety into the C3 position of quinoxalinone. | en_US |
dc.identifier.citation | Organic and Biomolecular Chemistry. Vol.16, No.15 (2018), 2697-2704 | en_US |
dc.identifier.doi | 10.1039/c8ob00375k | en_US |
dc.identifier.issn | 14770520 | en_US |
dc.identifier.other | 2-s2.0-85045841772 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/45274 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85045841772&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.title | Persulfate-promoted oxidative C-N bond coupling of quinoxalinones and: NH -sulfoximines | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85045841772&origin=inward | en_US |