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  <identifier identifierType="DOI">10.18453/rosdok_id00002477</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Garbe, Marcel</creatorName>
      <givenName>Marcel</givenName>
      <familyName>Garbe</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1190670313</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Manganese(I)-catalyzed (asymmetric) reduction of carbonyl bonds</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2019</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">2019</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00002477</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-rosdok_id00002477-9</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">This dissertation reports the synthesis of different non-noble metal complexes for the (asymmetric) reduction of predominantly ketones or esters to the corresponding alcohols. Thereby, mainly pincer ligands coordinated to a manganese(I) metal center were used while corresponding noble metal analogues already have demonstrated good activities in different reductions of organic compounds. Manganese(I) was used as a metal center because of its high abundance, low price and only minor toxicity in comparison to other noble metals.</description>
  </descriptions>
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