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  <identifier identifierType="DOI">10.18453/rosdok_id00000798</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Hussain, Munawar</creatorName>
      <givenName>Munawar</givenName>
      <familyName>Hussain</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/143545175</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Domino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-Tetrachloropyrimidine</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2010</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">2010</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00000798</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2011-0021-7</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">I have synthesized functionalized carbazoles and benzofurans based on domino twofold Heck / 6pi-electrocyclization reactions. Functionalized anthraquinones, fluorenones and benzocoumarines were also prepared by this methodology. Regioselctive Suzuki-Miyaura cross-coupling reactions of 2,4,5,6-tetrachloropyrimidine and 2,3,4,5-tetrabromofuran provided an expedient synthesis of mono-, di-, tri- and tetraaryl-pyrimidines and di- and tetraarylfurans.</description>
  </descriptions>
</resource>
