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Intramolecular Heterocyclization of O-Propargylated Aromatic Hydroxyaldehydes as an Expedient Route to Substituted Chromenopyridines under Metal-Free Conditions

Keskin, Selbi; Balci, Metin


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{
  "@context": "https://schema.org/", 
  "@id": 79515, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey", 
      "name": "Keskin, Selbi"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey", 
      "name": "Balci, Metin"
    }
  ], 
  "datePublished": "2015-01-01", 
  "description": "A concise and regioselective approach to the synthesis of chromenopyridine and chromenopyridinone derivatives was developed. The synthetic strategy relies on the O-propargylation of aromatic hydroxyaldehydes followed by reaction with propargylamine. The intramolecular cycloaddition reaction between the alkyne and azadiene, which is formed as an intermediate, furnished the desired skeletons.", 
  "headline": "Intramolecular Heterocyclization of O-Propargylated Aromatic Hydroxyaldehydes as an Expedient Route to Substituted Chromenopyridines under Metal-Free Conditions", 
  "identifier": 79515, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "Intramolecular Heterocyclization of O-Propargylated Aromatic Hydroxyaldehydes as an Expedient Route to Substituted Chromenopyridines under Metal-Free Conditions", 
  "url": "https://aperta.ulakbim.gov.tr/record/79515"
}
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