1 Ocak 2010 Dergi makalesi Açık Erişim

Artok, Levent; Kus, Melih; Urer, Bagdagul N.; Turkmen, Gulsah; Aksin-Artok, Ozge

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  "@context": "https://schema.org/", 
  "@id": 24485, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Izmir Inst Technol, Dept Chem, Fac Sci, TR-35430 Izmir, Turkey", 
      "name": "Artok, Levent"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Izmir Inst Technol, Dept Chem, Fac Sci, TR-35430 Izmir, Turkey", 
      "name": "Kus, Melih"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Izmir Inst Technol, Dept Chem, Fac Sci, TR-35430 Izmir, Turkey", 
      "name": "Urer, Bagdagul N."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Izmir Inst Technol, Dept Chem, Fac Sci, TR-35430 Izmir, Turkey", 
      "name": "Turkmen, Gulsah"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Dortmund Univ Technol, D-44227 Dortmund, Germany", 
      "name": "Aksin-Artok, Ozge"
    }
  ], 
  "datePublished": "2010-01-01", 
  "description": "Unsymmetric diynes possessing a terminal alkyne moiety reacted with organoboronic acids both chemo- and stereoselectively to afford arylated or alkenylated exocyclic dienes by catalysis from the [Rh(cod)OCH(3)](2) complex. The use of a polar protic solvent, e.g. CH(3)OH is required for the success of the process under mild conditions.", 
  "headline": "Rhodium catalysed chemo- and stereoselective arylative and alkenylative cyclisation reactions of unsymmetric diynes containing a terminal alkyne moiety with organoboronic acids", 
  "identifier": 24485, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "Rhodium catalysed chemo- and stereoselective arylative and alkenylative cyclisation reactions of unsymmetric diynes containing a terminal alkyne moiety with organoboronic acids", 
  "url": "https://aperta.ulakbim.gov.tr/record/24485"
}