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    <title>Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</title>
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    <namePart>Langer, Peter</namePart>
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    <namePart>Müller, Thomas J. J.</namePart>
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    <namePart>Mathematisch-Naturwissenschaftliche Fakultät</namePart>
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  <abstract type="Summary">The present thesis is mainly dedicated to the study of the synthesis of quinolines, pyrolo[2,3-b]indoles and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions. This includes arylation of quinolines via Suzuki-Miyaura and alkynylation of 4-trifluoromethylquinolines via Sonogashira reaction. Consequent synthesis of a wide range of fused pyridines and their further modifications were successfully performed. A number of pyrolo[2,3-b]indoles and pyrimido[4,5-b]indole-2,4(3H,9H)-diones were synthesized with the usage of Buchwald-Hartwig reaction.&lt;eng&gt;</abstract>
  <abstract type="Summary">Die vorliegende Arbeit beschäftigt sich mit der Synthese von Chinolinen, Pyrolo[2,3-b]indolen und 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-dionen durch Palladium-katalysierte Kreuzkupplungsreaktionen. Sie beinhaltet Arylierungen von Chinolinen mittels Suzuki-Miyaura-Reaktion und Alkinylierung von 4-Trifluoromethylchinolinen mittels Sonogashira-Reaktion. Außerdem wurden verschiedene Pyrolo[2,3-b]indole und Pyrimido[4,5-b]indole-2,4(3H,9H)-dione durch Buchwald-Hartwig-Reaktion hergestellt.&lt;ger&gt;</abstract>
  <note type="statement of responsibility">vorgelegt von M. Sc. Maksym Cherevatenko</note>
  <note type="thesis">Dissertation Universität Rostock 2017</note>
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      <title>Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</title>
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      <publisher>Rostock : Universität, 2017</publisher>
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      <form>207 Seiten</form>
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    <note>Druck-Ausgabe</note>
    <identifier type="local">(DE-627)1015123139</identifier>
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      <namePart>Cherevatenko, Maksym, 1988 - </namePart>
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  <identifier type="urn">urn:nbn:de:gbv:28-rosdok_id00002414-0</identifier>
  <identifier type="doi">10.18453/rosdok_id00002414</identifier>
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