Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:3735308rdf:typepubmed:Citationlld:pubmed
pubmed-article:3735308lifeskim:mentionsumls-concept:C0441655lld:lifeskim
pubmed-article:3735308lifeskim:mentionsumls-concept:C1280500lld:lifeskim
pubmed-article:3735308lifeskim:mentionsumls-concept:C0220781lld:lifeskim
pubmed-article:3735308lifeskim:mentionsumls-concept:C0026377lld:lifeskim
pubmed-article:3735308lifeskim:mentionsumls-concept:C1883254lld:lifeskim
pubmed-article:3735308lifeskim:mentionsumls-concept:C0360703lld:lifeskim
pubmed-article:3735308lifeskim:mentionsumls-concept:C0175815lld:lifeskim
pubmed-article:3735308pubmed:issue8lld:pubmed
pubmed-article:3735308pubmed:dateCreated1986-9-17lld:pubmed
pubmed-article:3735308pubmed:abstractTextThe syntheses of seven 4-(substituted phenyl)but-2-en(or yn)yl quaternary ammonium salts and four related tertiary amines are described. The Meerwein arylation reaction was the preferred synthetic method for the required intermediate 1-aryl-4-halo-2-butenes (15a-c, 18). In the case of 18, the trans stereochemistry of the Meerwein adduct of 2,3-dimethylbutadiene was established unambiguously by 2D NMR and X-ray studies. The title compounds represent conformationally restricted analogues of the class III antiarrhythmic agent clofilium (1) and exhibit comparable potency and efficacy in the in vitro evaluation using isolated canine Purkinje fibers. These results suggest that the alkylene chain in 1 is extended in the active conformation. Computer-aided conformational analysis (MM2) supports this conclusion. Selective catalytic hydrogen conditions were developed for the conversion of the unsaturated analogue 2 to clofilium (1) with minimal hydrogenolysis of the allylic quaternary ammonium moiety, thus completing a novel and efficient synthesis of this substance.lld:pubmed
pubmed-article:3735308pubmed:languageenglld:pubmed
pubmed-article:3735308pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3735308pubmed:citationSubsetIMlld:pubmed
pubmed-article:3735308pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3735308pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3735308pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3735308pubmed:statusMEDLINElld:pubmed
pubmed-article:3735308pubmed:monthAuglld:pubmed
pubmed-article:3735308pubmed:issn0022-2623lld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:LummaW CWCJrlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:WongS SSSlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:BriggsMMlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:SullivanM EMElld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:WanC NCNlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:DaveyD DDDlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:MorganT KTKJrlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:GomezR PRPlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:MariscaA JAJlld:pubmed
pubmed-article:3735308pubmed:authorpubmed-author:WohlR ARAlld:pubmed
pubmed-article:3735308pubmed:issnTypePrintlld:pubmed
pubmed-article:3735308pubmed:volume29lld:pubmed
pubmed-article:3735308pubmed:ownerNLMlld:pubmed
pubmed-article:3735308pubmed:authorsCompleteYlld:pubmed
pubmed-article:3735308pubmed:pagination1398-405lld:pubmed
pubmed-article:3735308pubmed:dateRevised2005-11-17lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:meshHeadingpubmed-meshheading:3735308-...lld:pubmed
pubmed-article:3735308pubmed:year1986lld:pubmed
pubmed-article:3735308pubmed:articleTitleSynthesis and class III antiarrhythmic activity of (phenylbut-2-enyl)ammonium salts. Effect of conformation on activity.lld:pubmed
pubmed-article:3735308pubmed:publicationTypeJournal Articlelld:pubmed
http://linkedlifedata.com/r...http://linkedlifedata.com/r...pubmed-article:3735308lld:chembl