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pubmed-article:19718728rdf:typepubmed:Citationlld:pubmed
pubmed-article:19718728lifeskim:mentionsumls-concept:C0002074lld:lifeskim
pubmed-article:19718728pubmed:issue38lld:pubmed
pubmed-article:19718728pubmed:dateCreated2009-9-28lld:pubmed
pubmed-article:19718728pubmed:abstractTextRecent breakthroughs have proved that direct palladium(II)-catalyzed allylic C-H alkylation can be achieved. This new procedure shows that the inherent requirement for a leaving group in the Tsuji-Trost palladium-catalyzed allylic alkylation can be lifted. These initial reports hold great promise for the development of allylic C-H alkylation into a widely applicable methodology, thus providing a means to enhance synthetic efficiency in these reactions.lld:pubmed
pubmed-article:19718728pubmed:languageenglld:pubmed
pubmed-article:19718728pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19718728pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:19718728pubmed:monthSeplld:pubmed
pubmed-article:19718728pubmed:issn1521-3765lld:pubmed
pubmed-article:19718728pubmed:authorpubmed-author:JensenThomasTlld:pubmed
pubmed-article:19718728pubmed:authorpubmed-author:FristrupPeter...lld:pubmed
pubmed-article:19718728pubmed:issnTypeElectroniclld:pubmed
pubmed-article:19718728pubmed:day28lld:pubmed
pubmed-article:19718728pubmed:volume15lld:pubmed
pubmed-article:19718728pubmed:ownerNLMlld:pubmed
pubmed-article:19718728pubmed:authorsCompleteYlld:pubmed
pubmed-article:19718728pubmed:pagination9632-6lld:pubmed
pubmed-article:19718728pubmed:year2009lld:pubmed
pubmed-article:19718728pubmed:articleTitleToward efficient palladium-catalyzed allylic C-H alkylation.lld:pubmed
pubmed-article:19718728pubmed:affiliationDepartment of Chemistry, Technical University of Denmark, Kemitorvet, building 207, Denmark.lld:pubmed
pubmed-article:19718728pubmed:publicationTypeJournal Articlelld:pubmed