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  <identifier identifierType="DOI">10.18453/rosdok_id00000748</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Prateeptongkum, Saisuree</creatorName>
      <givenName>Saisuree</givenName>
      <familyName>Prateeptongkum</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/143185101</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Iron-catalyzed C-N bond formations</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/id00000748</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2010-0172-1</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">This thesis is mainly concerned with the development and application of iron-catalyzed reactions for the synthesis of nitrogen-containing organic compounds. Oximes were synthesized by a novel iron-catalyzed nitrosation of olefins with tert-butyl nitrite and sodium borohydride. Succinimides and maleimides were prepared by employing an iron-catalyzed carbonylation of internal alkynes with ammonia as a key step. This efficient method was applied for the synthesis of natural products and interesting organic building blocks.</description>
  </descriptions>
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