Publication: 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.author | Praewpan Katrun | en_US |
dc.contributor.author | Chutima Kuhakarn | en_US |
dc.contributor.other | Khon Kaen University | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2020-01-27T07:46:11Z | |
dc.date.available | 2020-01-27T07:46:11Z | |
dc.date.issued | 2019-04-04 | en_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.citation | Tetrahedron Letters. Vol.60, No.14 (2019), 989-993 | en_US |
dc.identifier.doi | 10.1016/j.tetlet.2019.03.008 | en_US |
dc.identifier.issn | 18733581 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-85062459762 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/50205 | |
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=85062459762&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.title | 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 | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85062459762&origin=inward | en_US |