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pubmed-article:19388716rdf:typepubmed:Citationlld:pubmed
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pubmed-article:19388716pubmed:issue9lld:pubmed
pubmed-article:19388716pubmed:dateCreated2009-4-24lld:pubmed
pubmed-article:19388716pubmed:abstractTextThe direct oxidative coupling of 2-amino- and 2-hydroxybenzoic acids with internal alkynes proceeds efficiently in the presence of a rhodium/copper catalyst system under air to afford the corresponding 8-substituted isocoumarin derivatives, some of which exhibit solid-state fluorescence. Depending on conditions, 4-ethenylcarbazoles can be synthesized selectively from 2-(arylamino)benzoic acids. The oxidative coupling reactions of heteroarene carboxylic acids as well as aromatic diacids with an alkyne are also described.lld:pubmed
pubmed-article:19388716pubmed:languageenglld:pubmed
pubmed-article:19388716pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19388716pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:19388716pubmed:monthMaylld:pubmed
pubmed-article:19388716pubmed:issn1520-6904lld:pubmed
pubmed-article:19388716pubmed:authorpubmed-author:HiranoKojiKlld:pubmed
pubmed-article:19388716pubmed:authorpubmed-author:SatohTetsuyaTlld:pubmed
pubmed-article:19388716pubmed:authorpubmed-author:MiuraMasahiro...lld:pubmed
pubmed-article:19388716pubmed:authorpubmed-author:ShimizuMasaki...lld:pubmed
pubmed-article:19388716pubmed:issnTypeElectroniclld:pubmed
pubmed-article:19388716pubmed:day1lld:pubmed
pubmed-article:19388716pubmed:volume74lld:pubmed
pubmed-article:19388716pubmed:ownerNLMlld:pubmed
pubmed-article:19388716pubmed:authorsCompleteYlld:pubmed
pubmed-article:19388716pubmed:pagination3478-83lld:pubmed
pubmed-article:19388716pubmed:year2009lld:pubmed
pubmed-article:19388716pubmed:articleTitleWaste-free synthesis of condensed heterocyclic compounds by rhodium-catalyzed oxidative coupling of substituted arene or heteroarene carboxylic acids with alkynes.lld:pubmed
pubmed-article:19388716pubmed:affiliationDepartment of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.lld:pubmed
pubmed-article:19388716pubmed:publicationTypeJournal Articlelld:pubmed