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    <title>Synthesis of functionalized pyridines and quinolines by palladium-catalyzed cross-coupling reactions</title>
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  <abstract type="Summary">This thesis deals with the functionalization of pentahalogenated pyridines and dihalogenated quinolines through palladium catalyzed cross coupling reactions. This includes the chemo-selective arylation and alkynylation of 4-bromo-2,3,5-trichloro-6-iodopyridine using Suzuki and Sonogashira reactions. The chemo-selective arylation of 4,6-dihalogenated-2-(trifluoromethyl)quinoline by Suzuki reaction was studied. Besides, the synthesis of indolo [2,3-c]quinolines was studied by sequential chemo-selective Suzuki reaction followed by double C-N coupling starting from 3-bromo-4-iodoquinoline.&lt;eng&gt;</abstract>
  <note type="statement of responsibility">vorgelegt von Rodisnel Perdomo Rivera</note>
  <note>GutachterInnen: Peter Langer (Universität Rostock, Institut für Chemie) ; Bernd Schmidt (Universität Potsdam, Institut für Chemie)</note>
  <note type="thesis">Dissertation Universität Rostock 2018</note>
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      <title>Synthesis of functionalized pyridines and quinolines by palladium-catalyzed cross-coupling reactions</title>
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