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pubmed-article:17914837rdf:typepubmed:Citationlld:pubmed
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pubmed-article:17914837pubmed:issue22lld:pubmed
pubmed-article:17914837pubmed:dateCreated2007-10-18lld:pubmed
pubmed-article:17914837pubmed:abstractTextCationic palladium(II) ([Pd(MeCN)4](BF4)2) provides the first transition-metal-catalyzed method for electrophilic activation of electron-deficient 1,1-difluoro-1-alkenes, which allows their Friedel-Crafts-type cyclization with an intramolecular aryl group via a Wacker-type process. By using BF3.OEt2, the cyclization was effected by a catalytic amount of the palladium without its reoxidation.lld:pubmed
pubmed-article:17914837pubmed:languageenglld:pubmed
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pubmed-article:17914837pubmed:issn1523-7060lld:pubmed
pubmed-article:17914837pubmed:authorpubmed-author:IchikawaJunji...lld:pubmed
pubmed-article:17914837pubmed:authorpubmed-author:YokotaMisakiMlld:pubmed
pubmed-article:17914837pubmed:authorpubmed-author:FujitaDaishiDlld:pubmed
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pubmed-article:17914837pubmed:volume9lld:pubmed
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pubmed-article:17914837pubmed:pagination4639-42lld:pubmed
pubmed-article:17914837pubmed:year2007lld:pubmed
pubmed-article:17914837pubmed:articleTitleActivation of 1,1-difluoro-1-alkenes with a transition-metal complex: palladium(II)-catalyzed Friedel-Crafts-type cyclization of 4,4-(difluorohomoallyl)arenes.lld:pubmed
pubmed-article:17914837pubmed:affiliationDepartment of Chemistry, Graduate School of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8571, Japan.lld:pubmed
pubmed-article:17914837pubmed:publicationTypeJournal Articlelld:pubmed