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pubmed-article:18452005rdf:typepubmed:Citationlld:pubmed
pubmed-article:18452005lifeskim:mentionsumls-concept:C0016327lld:lifeskim
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pubmed-article:18452005pubmed:issue10lld:pubmed
pubmed-article:18452005pubmed:dateCreated2008-5-2lld:pubmed
pubmed-article:18452005pubmed:abstractTextThe electrophilic fluorodesilylation of enantioenriched allenylsilanes proceeds with efficient transfer of chirality. The silylation-fluorination of propargylic alcohols occurs with overall retention of stereochemistry, a result consistent with a stereospecific anti S(E)2' mechanism for the fluorination step.lld:pubmed
pubmed-article:18452005pubmed:languageenglld:pubmed
pubmed-article:18452005pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18452005pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:18452005pubmed:monthMaylld:pubmed
pubmed-article:18452005pubmed:issn1477-0520lld:pubmed
pubmed-article:18452005pubmed:authorpubmed-author:ReayW AWAlld:pubmed
pubmed-article:18452005pubmed:authorpubmed-author:GouverneurVér...lld:pubmed
pubmed-article:18452005pubmed:authorpubmed-author:ClaridgeTimot...lld:pubmed
pubmed-article:18452005pubmed:authorpubmed-author:CarrollLauren...lld:pubmed
pubmed-article:18452005pubmed:authorpubmed-author:McCulloughSam...lld:pubmed
pubmed-article:18452005pubmed:issnTypePrintlld:pubmed
pubmed-article:18452005pubmed:day21lld:pubmed
pubmed-article:18452005pubmed:volume6lld:pubmed
pubmed-article:18452005pubmed:ownerNLMlld:pubmed
pubmed-article:18452005pubmed:authorsCompleteYlld:pubmed
pubmed-article:18452005pubmed:pagination1731-3lld:pubmed
pubmed-article:18452005pubmed:year2008lld:pubmed
pubmed-article:18452005pubmed:articleTitleStereospecific anti SE2' fluorination of allenylsilanes: synthesis of enantioenriched propargylic fluorides.lld:pubmed
pubmed-article:18452005pubmed:affiliationUniversity of Oxford, Chemistry Research Laboratory, 12 Mansfield Road, Oxford, UK OX1 3TA.lld:pubmed
pubmed-article:18452005pubmed:publicationTypeJournal Articlelld:pubmed