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  <identifier identifierType="DOI">10.18453/rosdok_id00000733</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Asad, Ali</creatorName>
      <givenName>Ali</givenName>
      <familyName>Asad</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/142870900</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Synthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling Reactions</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/id00000733</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2010-0156-3</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">Sterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products.</description>
  </descriptions>
</resource>
