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pubmed-article:15524483rdf:typepubmed:Citationlld:pubmed
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pubmed-article:15524483pubmed:issue23lld:pubmed
pubmed-article:15524483pubmed:dateCreated2004-11-4lld:pubmed
pubmed-article:15524483pubmed:abstractTextTreatment of alpha,beta-unsaturated ketones with CF(3)I in the presence of Et(2)Zn and RhCl(PPh(3))(3) gave novel alpha-trifluoromethylation products in good yields. Hydrogen transfer from the ethyl group on the rhodium complex to the beta-position of the enone seems to play an important role in this reaction.lld:pubmed
pubmed-article:15524483pubmed:languageenglld:pubmed
pubmed-article:15524483pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15524483pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:15524483pubmed:monthNovlld:pubmed
pubmed-article:15524483pubmed:issn1523-7060lld:pubmed
pubmed-article:15524483pubmed:authorpubmed-author:AndoAkiraAlld:pubmed
pubmed-article:15524483pubmed:authorpubmed-author:SatoKazuyukiKlld:pubmed
pubmed-article:15524483pubmed:authorpubmed-author:OmoteMasaakiMlld:pubmed
pubmed-article:15524483pubmed:authorpubmed-author:KumadakiItsum...lld:pubmed
pubmed-article:15524483pubmed:issnTypePrintlld:pubmed
pubmed-article:15524483pubmed:day11lld:pubmed
pubmed-article:15524483pubmed:volume6lld:pubmed
pubmed-article:15524483pubmed:ownerNLMlld:pubmed
pubmed-article:15524483pubmed:authorsCompleteYlld:pubmed
pubmed-article:15524483pubmed:pagination4359-61lld:pubmed
pubmed-article:15524483pubmed:year2004lld:pubmed
pubmed-article:15524483pubmed:articleTitleRhodium-catalyzed novel trifluoromethylation at the alpha-position of alpha,beta-unsaturated ketones.lld:pubmed
pubmed-article:15524483pubmed:affiliationFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka 573-0101, Japan.lld:pubmed
pubmed-article:15524483pubmed:publicationTypeJournal Articlelld:pubmed