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  <identifier identifierType="DOI">10.18453/rosdok_id00004888</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Sobhani, Maryam</creatorName>
      <givenName>Maryam</givenName>
      <familyName>Sobhani</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1372671455</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Alkyne-carbonyl metathesis reaction in polycyclic synthesis</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2024</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">2024</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">https://purl.uni-rostock.de/rosdok/id00004888</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-rosdok_id00004888-1</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">The aim of this dissertation is to develop an efficient methodology for the design of several new carbo- and heterocycles. The focus is on using Alkyne-Carbonyl Metathesis (ACM) reaction due to its high atom economy and efficiency. In this regard, a metal free, Brønsted acid mediated intramolecular ACM reaction has been developed to form new seven- and six-membered carbocycles. In general, regio- and chemoselective palladium-catalyzed cross-coupling reactions with various boronic acids and alkynes were applied in all studies to synthesize the precursors for the ring closing ACM reaction.</description>
  </descriptions>
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