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K <inf>2</inf> S <inf>2</inf> O <inf>8</inf> -Mediated halogenation of 2-arylimidazo[1,2-a]pyridines using sodium halides as the halogen sources

dc.contributor.authorPraewpan Katrunen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-01-27T07:46:11Z
dc.date.available2020-01-27T07:46:11Z
dc.date.issued2019-04-04en_US
dc.description.abstract© 2019 Elsevier Ltd A convenient halogenation of 2-arylimidazo[1,2-a]pyridines using sodium chloride/bromide/iodide as the halogen sources in the presence of K 2 S 2 O 8 as an easy-to-handle oxidizing agent was developed. The present work offers an efficient and rapid access to 3-chloro-, 3-bromo- and 3-iodo-2-arylimidazo[1,2-a]pyridines which can be readily converted to C3-substituted imidazo[1,2-a]pyridines by cross-coupling reactions.en_US
dc.identifier.citationTetrahedron Letters. Vol.60, No.14 (2019), 989-993en_US
dc.identifier.doi10.1016/j.tetlet.2019.03.008en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-85062459762en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/50205
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85062459762&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleK <inf>2</inf> S <inf>2</inf> O <inf>8</inf> -Mediated halogenation of 2-arylimidazo[1,2-a]pyridines using sodium halides as the halogen sourcesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85062459762&origin=inwarden_US

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