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A novel DMSO-assisted regioselective iodination of aniline analogues

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dc.contributor.authorPakorn Bovonsombaten_US
dc.contributor.authorWanutcha Lorpaiboonen_US
dc.contributor.authorSarocha Laoboonchaien_US
dc.contributor.authorPrima Sriprachaya-anunten_US
dc.contributor.authorWarangkana Yimkosolen_US
dc.contributor.authorNatthapatch Siriphatcharachaikulen_US
dc.contributor.authorPornpawit Siricharoensangen_US
dc.contributor.authorTerawee Kangwannarakulen_US
dc.contributor.authorJin Maedaen_US
dc.contributor.authorSatreerat Losuwanakulen_US
dc.contributor.authorMaitraye Mahesh Abhyankaren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-10-05T04:12:58Z
dc.date.available2020-10-05T04:12:58Z
dc.date.issued2020-01-01en_US
dc.description.abstract© 2020 Elsevier Ltd A metal- and oxidant-free electrophilic iodination of aniline analogues was achieved in high to excellent yields at room temperature in MTBE with 0 or 3.5 equivalents of DMSO. Examined substituents include N-alkyl, N,N-dialkyl, N-morpholinyl and N-piperazinyl as well as methyl, Br, CN and CO2CH3 aryl ring substitutions.en_US
dc.identifier.citationTetrahedron Letters. (2020)en_US
dc.identifier.doi10.1016/j.tetlet.2020.152461en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-85091223010en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/58983
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85091223010&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleA novel DMSO-assisted regioselective iodination of aniline analoguesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85091223010&origin=inwarden_US

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