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  <identifier identifierType="DOI">10.18453/rosdok_id00000914</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Bunescu, Alina</creatorName>
      <givenName>Alina</givenName>
      <familyName>Bunescu</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1016859198</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Bis-silyl-enol ethers as convenient building blocks for the design and synthesis of Salicylates, Pyrones, Cyclohexenones, Pyridones and Benzophenones</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2011</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">2011</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00000914</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2011-0146-3</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">The present thesis describes the synthetic potential of 1,3-bis-silyl-enol ethers. They undergo regioselective cyclocondensation reactions with simple substrates providing various complex carba- and heterocycles. A new type of formal [3+3]-cyclization reaction with 2,4,6-tris(trifluoromethyl)-1,3,5-triazine is described. The mechanism was studied by the isolation of an unusual bicyclic intermediate. New and promising candidates for UV-A/B filters have been synthesized and analyzed.</description>
  </descriptions>
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