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  <identifier identifierType="DOI">10.18453/rosdok_id00002482</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Kuhrt, Katharina</creatorName>
      <givenName>Katharina</givenName>
      <familyName>Kuhrt</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1190655349</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Investigation on new tertiary P-chirogenic di(triaryl phosphines)</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2018</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">2018</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00002482</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-rosdok_id00002482-3</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">In this thesis, the synthesis of numerous di(triaryl phosphines) with DPE- or DBF-backbone was investigated using the well-known (-)-ephedrine methodology established by S. Jugé and co-workers. These di(triaryl phosphines) were tested in asymmetric catalysis and examined in regard to their stereochemical stability. Additionally, a new route for the synthesis of a P-chirogenic BINAP-type di(triaryl phosphine) was developed starting from a P-chirogenic secondary phosphine borane.</description>
  </descriptions>
</resource>
