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pubmed-article:14995184rdf:typepubmed:Citationlld:pubmed
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pubmed-article:14995184pubmed:issue9lld:pubmed
pubmed-article:14995184pubmed:dateCreated2004-3-3lld:pubmed
pubmed-article:14995184pubmed:abstractTextThe rhodium-catalyzed carbonylative [3+2+1] cycloaddition of trienes into bicyclohexenones has been developed. The carbonylated cycloaddition products have a high regioselectivity. This catalytic system tolerates functionalities including ether, sulfonamide, and ester.lld:pubmed
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pubmed-article:14995184pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:14995184pubmed:monthMarlld:pubmed
pubmed-article:14995184pubmed:issn0002-7863lld:pubmed
pubmed-article:14995184pubmed:authorpubmed-author:LeeSang IckSIlld:pubmed
pubmed-article:14995184pubmed:authorpubmed-author:ChungYoung...lld:pubmed
pubmed-article:14995184pubmed:authorpubmed-author:LeeSueg-GeunS...lld:pubmed
pubmed-article:14995184pubmed:authorpubmed-author:ParkJi HoonJHlld:pubmed
pubmed-article:14995184pubmed:issnTypePrintlld:pubmed
pubmed-article:14995184pubmed:day10lld:pubmed
pubmed-article:14995184pubmed:volume126lld:pubmed
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pubmed-article:14995184pubmed:pagination2714-5lld:pubmed
pubmed-article:14995184pubmed:dateRevised2008-1-17lld:pubmed
pubmed-article:14995184pubmed:year2004lld:pubmed
pubmed-article:14995184pubmed:articleTitleRhodium-catalyzed carbonylative [2+2+1] cycloaddition reactions: catalytic formation of bicyclic cyclohexenones [corrected].lld:pubmed
pubmed-article:14995184pubmed:affiliationSchool of Chemistry and Center for Molecular Catalysis, Seoul National University, Seoul 151-747, Korea.lld:pubmed
pubmed-article:14995184pubmed:publicationTypeJournal Articlelld:pubmed
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