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  <identifier identifierType="DOI">10.18453/rosdok_id00001587</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Khaddour, Zien</creatorName>
      <givenName>Zien</givenName>
      <familyName>Khaddour</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1075020468</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Synthesis of functionalized naphthalenes, coumarines, quinolines, and isoflavones by chemo- and site-selective palladium-catalyzed coupling reactions</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2015</publicationYear>
  <resourceType resourceTypeGeneral="Text" />
  <subjects>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">540 Chemistry &amp; allied sciences</subject>
  </subjects>
  <dates>
    <date dateType="Created">2015</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00001587</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2015-0137-3</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">I studied the site-selectivity of Suzuki cross-coupling reactions of the bis(triflate) of naphthoates, coumarines, and isoflavones. In addition, the chemo-selectivity of Suzuki cross-coupling reactions of naphthoates and quinolones containing bromide and triflate leaving groups were studied. In this context, were prepared various arylated pharmacologically relevant heterocycles which are not readily available by other synthetic methods.</description>
  </descriptions>
</resource>
