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pubmed-article:12778709rdf:typepubmed:Citationlld:pubmed
pubmed-article:12778709lifeskim:mentionsumls-concept:C0443286lld:lifeskim
pubmed-article:12778709lifeskim:mentionsumls-concept:C0205250lld:lifeskim
pubmed-article:12778709pubmed:issue10lld:pubmed
pubmed-article:12778709pubmed:dateCreated2003-6-3lld:pubmed
pubmed-article:12778709pubmed:abstractTextHighly diastereoselective Lewis acid mediated aza-Diels-Alder reactions of chiral auxiliary derivatized 2H-azirines have been accomplished for the first time, yielding bi and tri-cyclic heterocyclic compounds, comprising aziridine and tetrahydropyridine substructures, in up to 97% de; with the absolute stereochemistry of the major product confirmed by X-ray crystallography.lld:pubmed
pubmed-article:12778709pubmed:languageenglld:pubmed
pubmed-article:12778709pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12778709pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:12778709pubmed:monthMaylld:pubmed
pubmed-article:12778709pubmed:issn1359-7345lld:pubmed
pubmed-article:12778709pubmed:authorpubmed-author:FischerAndrea...lld:pubmed
pubmed-article:12778709pubmed:authorpubmed-author:SomfaiPeterPlld:pubmed
pubmed-article:12778709pubmed:authorpubmed-author:TiménAsa...lld:pubmed
pubmed-article:12778709pubmed:issnTypePrintlld:pubmed
pubmed-article:12778709pubmed:day21lld:pubmed
pubmed-article:12778709pubmed:ownerNLMlld:pubmed
pubmed-article:12778709pubmed:authorsCompleteYlld:pubmed
pubmed-article:12778709pubmed:pagination1150-1lld:pubmed
pubmed-article:12778709pubmed:year2003lld:pubmed
pubmed-article:12778709pubmed:articleTitleStereoselective aza-Diels-Alder reactions with 2H-azirines as dienophiles furnishing highly functionalized tetrahydropyridines.lld:pubmed
pubmed-article:12778709pubmed:affiliationDepartment of Chemistry, Royal Institute of Technology, S-100 44 Stockholm, Sweden.lld:pubmed
pubmed-article:12778709pubmed:publicationTypeJournal Articlelld:pubmed