Publication:
Reaction of some 4,6-dimethoxyindoles with nitric acid: Nitration and oxidative dimerisation

dc.contributor.authorTinnagon Keawinen_US
dc.contributor.authorShuleewan Rajviroongiten_US
dc.contributor.authorDavid Stc Blacken_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of New South Wales (UNSW) Australiaen_US
dc.date.accessioned2018-06-21T08:10:14Z
dc.date.available2018-06-21T08:10:14Z
dc.date.issued2005-01-24en_US
dc.description.abstractA range of 3-substituted-4,6-dimethoxyindoles bearing electron-withdrawing groups in either the 2- or 7-position, can be nitrated using nitric acid in acetonitrile, to give 7-nitro and 2-nitro-indoles, respectively. Those without electron-withdrawing groups undergo oxidative dimerisation at C7, if 2,3-disubstituted, and at C2, if N-methylated and unsubstituted at C2. Some 3-substituted-4,6-dimethoxyindoles can be nitrated using nitric acid in acetonitrile, to give 7-nitro and 2-nitro-indoles. Some undergo oxidative dimerisation at C7, if 2,3-disubstituted, and at C2, if N-methylated and unsubstituted at C2. © 2004 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron. Vol.61, No.4 (2005), 853-861en_US
dc.identifier.doi10.1016/j.tet.2004.11.026en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-11144298661en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/16381
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=11144298661&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleReaction of some 4,6-dimethoxyindoles with nitric acid: Nitration and oxidative dimerisationen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=11144298661&origin=inwarden_US

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