Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:17508762rdf:typepubmed:Citationlld:pubmed
pubmed-article:17508762lifeskim:mentionsumls-concept:C0598128lld:lifeskim
pubmed-article:17508762lifeskim:mentionsumls-concept:C1527177lld:lifeskim
pubmed-article:17508762lifeskim:mentionsumls-concept:C0441513lld:lifeskim
pubmed-article:17508762lifeskim:mentionsumls-concept:C0332219lld:lifeskim
pubmed-article:17508762pubmed:issue12lld:pubmed
pubmed-article:17508762pubmed:dateCreated2007-6-1lld:pubmed
pubmed-article:17508762pubmed:abstractTextThe simple refluxing of allenynes, having a phenylsulfonyl functionality on the allenyl group, in xylene (or mesitylene) without microwave irradiation resulted in the efficient formation of bicyclo[5.2.0]nona-1,7-dienes and bicyclo[4.2.0]octa-1,6-dienes in high yields. This method was shown to be successfully applicable to the first construction of bicyclo[6.2.0]deca-1,8-dienes. Construction of the corresponding oxa- and azabicyclo[m.2.0] frameworks could also be attained. This thermal ring-closing reaction involves the formal [2+2] cycloaddition in which the distal double bond of an allenyl moiety exclusively served as one of the pi-components regardless of the position of the phenysulfonyl functionality on the allenyl moiety.lld:pubmed
pubmed-article:17508762pubmed:languageenglld:pubmed
pubmed-article:17508762pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17508762pubmed:citationSubsetIMlld:pubmed
pubmed-article:17508762pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17508762pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17508762pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17508762pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17508762pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17508762pubmed:statusMEDLINElld:pubmed
pubmed-article:17508762pubmed:monthJunlld:pubmed
pubmed-article:17508762pubmed:issn0022-3263lld:pubmed
pubmed-article:17508762pubmed:authorpubmed-author:InagakiFuyuhi...lld:pubmed
pubmed-article:17508762pubmed:authorpubmed-author:MukaiChisatoClld:pubmed
pubmed-article:17508762pubmed:authorpubmed-author:MiyashitaYusu...lld:pubmed
pubmed-article:17508762pubmed:authorpubmed-author:HaraYasuyukiYlld:pubmed
pubmed-article:17508762pubmed:issnTypePrintlld:pubmed
pubmed-article:17508762pubmed:day8lld:pubmed
pubmed-article:17508762pubmed:volume72lld:pubmed
pubmed-article:17508762pubmed:ownerNLMlld:pubmed
pubmed-article:17508762pubmed:authorsCompleteYlld:pubmed
pubmed-article:17508762pubmed:pagination4454-61lld:pubmed
pubmed-article:17508762pubmed:meshHeadingpubmed-meshheading:17508762...lld:pubmed
pubmed-article:17508762pubmed:meshHeadingpubmed-meshheading:17508762...lld:pubmed
pubmed-article:17508762pubmed:meshHeadingpubmed-meshheading:17508762...lld:pubmed
pubmed-article:17508762pubmed:meshHeadingpubmed-meshheading:17508762...lld:pubmed
pubmed-article:17508762pubmed:meshHeadingpubmed-meshheading:17508762...lld:pubmed
pubmed-article:17508762pubmed:year2007lld:pubmed
pubmed-article:17508762pubmed:articleTitleThermal [2+2] cycloaddition of allenynes: easy construction of bicyclo[6.2.0]deca-1,8-dienes, bicyclo[5.2.0]nona-1,7-dienes, and bicyclo[4.2.0]octa-1,6-dienes.lld:pubmed
pubmed-article:17508762pubmed:affiliationDivision of Pharmaceutical Sciences, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan. cmukai@kenroku.kanazawa-u.ac.jplld:pubmed
pubmed-article:17508762pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17508762pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17508762lld:pubmed