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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4594
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dc.contributor.authorCrisp, Geoffrey T.en
dc.contributor.authorTurner, Peter Daviden
dc.contributor.authorStephens, Kim A.en
dc.date.issued1998en
dc.identifier.citationJournal of Organometallic Chemistry, 1998; 570(2):219-224en
dc.identifier.issn0022-328Xen
dc.identifier.urihttp://hdl.handle.net/2440/4594-
dc.description.abstractThe palladium-catalysed coupling of aryl halides with terminal alkynes can be performed using base, zinc chloride and sodium iodide. This protocol represents a convenient method for the generation of nucleophilic acetylides in situ.en
dc.description.statementofresponsibilityGeoffrey T Crisp, Peter D Turner, Kim A Stephensen
dc.language.isoenen
dc.rightsCopyright © 1998 Elsevier Science S.A. All rights reserved.en
dc.subjectPalladium catalysis; Coupling of oxyhalides with alkynes; Nucleophilic alkynesen
dc.titlePalladium-catalysed coupling of terminal alkynes with aryl halides aided by catalytic zincen
dc.typeJournal articleen
dc.contributor.schoolSchool of Chemistry and Physics : Chemistryen
dc.identifier.doi10.1016/S0022-328X(98)00765-7en
Appears in Collections:Chemistry publications

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