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New protocols for the synthesis of 3,4-annulated and 4-substituted quinolines from β-bromo α,β-unsaturated aldehydes and 1-bromo-2-nitrobenzene or 2-bromoacetanilide

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dc.contributor.authorSome, Surajit
dc.contributor.authorRay, Jayanta K
dc.contributor.authorBanwell, Martin
dc.contributor.authorJones, Matthew
dc.date.accessioned2015-12-07T22:50:16Z
dc.date.issued2007
dc.date.updated2015-12-07T12:16:03Z
dc.description.abstractThe palladium[0]-mediated Ullmann cross-coupling of readily available β-bromo-α,β-unsaturated aldehydes of the general form 2 with 1-bromo-2-nitrobenzene (3, X = Br) delivers products, 4, that undergo reductive cyclization to novel quinolines (5) upon
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/1885/26960
dc.publisherElsevier
dc.sourceTetrahedron Letters
dc.subjectKeywords: acetanilide derivative; aldehyde derivative; ammonium chloride; bromine derivative; indium; nickel; nitrobenzene derivative; palladium; potassium carbonate; quinoline derivative; annulation reaction; aqueous solution; article; cross coupling reaction; cyc Quinolines; Reductive cyclization; Ullmann reaction; Vilsmeier-Haack haloformylation
dc.titleNew protocols for the synthesis of 3,4-annulated and 4-substituted quinolines from β-bromo α,β-unsaturated aldehydes and 1-bromo-2-nitrobenzene or 2-bromoacetanilide
dc.typeJournal article
local.bibliographicCitation.issue20
local.bibliographicCitation.lastpage3612
local.bibliographicCitation.startpage3609
local.contributor.affiliationSome, Surajit, Indian Institute of Technology
local.contributor.affiliationRay, Jayanta K, Indian Institute of Technology
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationJones, Matthew, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidJones, Matthew, u4193049
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB48
local.identifier.citationvolume48
local.identifier.doi10.1016/j.tetlet.2007.03.078
local.identifier.scopusID2-s2.0-34247169118
local.type.statusPublished Version

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