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    <title>Synthesis of substituted 1-deazapurines via Pd/Cu catalysed C-H activation, substituted naphthyridines, quinoxalines, and trifluoromethyl-substituted arenes by Pd(0)-catalysed cross-coupling reactions</title>
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    <namePart>Ali, Iftikhar</namePart>
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  <abstract type="Summary">The Pd/Cu catalyzed reactions of 3H-imidazo[4,5-b]pyridines (1-deazapurines) via C-H bond activation provided arylated 1-deazapurines. The arylation took place at position 2 of the 1-deazapurines. Pd(0)-catalysed Suzuki-Miyaura cross coupling reactions of 5,7-dichloro-1,6-naphthyridine, 2,6-dichloroquinoxaline and 2,4-dichloro-1-(trifluoromethyl)benzene with different arylboronic acids afforded aryl-substituted naphthyridines, quinoxalines and trifluoromethyl-substituted di- and terphenyls with excellent site-selectivity. The first attack occurred at the more electronically deficient and sterically less hindered position.</abstract>
  <note type="statement of responsibility">vorgelegt von Iftikhar Ali</note>
  <note type="thesis">Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2012</note>
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      <title>Synthesis of substituted 1-deazapurines via Pd/Cu catalysed C-H activation, substituted naphthyridines, quinoxalines, and trifluoromethyl-substituted arenes by Pd(0)-catalysed cross-coupling reactions</title>
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      <form>[5], III, 135 Bl.</form>
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