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Microwave-assisted trans -halogenation reactions of various chloro-, bromo-, trifluoromethanesulfonyloxy- and nonafluorobutanesulfonyloxy-substituted quinolines, isoquinolines, and pyridines leading to the corresponding iodinated heterocycles

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dc.contributor.authorBissember, Alexander
dc.contributor.authorBanwell, Martin
dc.date.accessioned2015-12-10T22:30:33Z
dc.date.issued2009
dc.date.updated2016-02-24T10:23:02Z
dc.description.abstract(Chemical Equation Presented) Microwave irradiation of certain chloro-, bromo-, trifluoromethanesulfonyloxy- and nonafluorobutanesulfonyloxy-substituted quinolines in the presence of acetic anhydride and sodium iodide leads, via a trans-halogenation process, to the corresponding iodides in high yield. Related conversions involving pyridines and isoquinolines can also be achieved under similar conditions.
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/1885/55143
dc.publisherAmerican Chemical Society
dc.sourceJournal of Organic Chemistry
dc.subjectKeywords: Acetic anhydrides; Chemical equations; Heterocycles; High yield; Isoquinolines; Microwave-assisted; Sodium iodides; Halogenation; Pyridine; Sodium; Microwave irradiation; acetic anhydride; heterocyclic compound; isoquinoline derivative; methyl bromide; me
dc.titleMicrowave-assisted trans -halogenation reactions of various chloro-, bromo-, trifluoromethanesulfonyloxy- and nonafluorobutanesulfonyloxy-substituted quinolines, isoquinolines, and pyridines leading to the corresponding iodinated heterocycles
dc.typeJournal article
local.bibliographicCitation.issue13
local.bibliographicCitation.lastpage4895
local.bibliographicCitation.startpage4893
local.contributor.affiliationBissember, Alexander, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBissember, Alexander, u3951047
local.contributor.authoruidBanwell, Martin, u9500594
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB320
local.identifier.citationvolume74
local.identifier.doi10.1021/jo9008386
local.identifier.scopusID2-s2.0-67649588596
local.identifier.thomsonID000267432700033
local.type.statusPublished Version

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