1 Ocak 2015 Dergi makalesi Açık Erişim

Keskin, Selbi; Balci, Metin

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/79515</identifier>
  <creators>
    <creator>
      <creatorName>Keskin, Selbi</creatorName>
      <givenName>Selbi</givenName>
      <familyName>Keskin</familyName>
      <affiliation>Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Balci, Metin</creatorName>
      <givenName>Metin</givenName>
      <familyName>Balci</familyName>
      <affiliation>Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Intramolecular Heterocyclization Of O-Propargylated Aromatic Hydroxyaldehydes As An Expedient Route To Substituted Chromenopyridines Under Metal-Free Conditions</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2015</publicationYear>
  <dates>
    <date dateType="Issued">2015-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/79515</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1021/acs.orglett.5b00067</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
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  <descriptions>
    <description descriptionType="Abstract">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.</description>
  </descriptions>
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