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Directed deprotonation-transmetallation of 4-bromopyridine: Flexible routes to substituted pyridines

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dc.contributor.authorGunter Karigen_US
dc.contributor.authorNopporn Thasanaen_US
dc.contributor.authorTimothy Gallagheren_US
dc.contributor.otherUniversity of Bristolen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T02:58:45Z
dc.date.available2018-07-24T02:58:45Z
dc.date.issued2002-05-20en_US
dc.description.abstractHalide-directed deprotonation and Li-Zn exchange of 4-bromopyridine 4 provides organozinc 6, which undergoes Pd-mediated coupling to give the 3-aryl-4-bromopyridines 7. Further substitution is achieved to provide the 3,4-disubstituted pyridines 8 and 9, and the 3,4,5-trisubstituted variants 10.en_US
dc.identifier.citationSynlett. No.5 (2002), 808-810en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-0036250925en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/20129
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036250925&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleDirected deprotonation-transmetallation of 4-bromopyridine: Flexible routes to substituted pyridinesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036250925&origin=inwarden_US

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