<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Synthese polycyclischer aromatischer Stickstoff-Heterocyclen: Verwendung von Palladium-katalysierten Kupplungsreaktionen und Lewis-Säure vermittelter Cycloisomerisierung</dc:title>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Parpart, Silvio , 1988- (VerfasserIn)</dc:contributor>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Langer, Peter , 1969- (AkademischeR BetreuerIn)</dc:contributor>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Schmidt, Berndt (AkademischeR BetreuerIn)</dc:contributor>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Universität Rostock (Grad-verleihende Institution)</dc:contributor>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät (Grad-verleihende Institution)</dc:contributor>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">Text</dc:type>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">theses</dc:type>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">Text</dc:type>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">Hochschulschrift</dc:type>
  <dc:date xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">2018</dc:date>
  <dc:date xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">2018</dc:date>
  <dc:language xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">ger</dc:language>
  <dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">electronic resource</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">remote</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">Computermedien</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">Online-Ressource</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">1 Online-Ressource</dc:format>
  <dc:description xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Die vorliegende Arbeit beschreibt die Synthese von Thieno[3,2-b]indolen, Pyrrolo[1,2 a][1,8]naphthyridinen, Pyrrolo[1,2-a][1,6]naphthyridinen sowie Indolizino[6,5,4,3-ija][1,6]naphthyridinen. Zum Aufbau der polycyclischen Systeme wurden vorwiegend Palladium-katalysierte Kupplungsreaktionen (Suzuki Reaktion, Sonogashira Reaktion, Buchwald-Hartwig-Kupplung) sowie Cycloisomerisierungs-Reaktionen (Ringschluss Alkin-Carbonyl-Metathese, intramolekulare elektrophile aromatische Substitution) verwendet.&lt;ger&gt;</dc:description>
  <dc:description xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">The present thesis deals with the synthesis of thieno[3,2-b]indoles, pyrrolo[1,2-a][1,8]naphthyridines, pyrrolo[1,2-a][1,6]naphthyridines as well as indolizino[6,5,4,3-ija][1,6]naphthyridines. All starting materials are easy available building-blocks. To prepare the polycyclic compounds, especially palladium-catalyzed cross-coupling reactions (Suzuki reaction, Sonogashira reaction, Buchwald-Hartwig amination) and cycloisomerization reactions (ring-closing alkyne-carbonyl-metathesis, intramolecular electrophilic aromatic substitution) were used.&lt;eng&gt;</dc:description>
  <dc:description xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">von M.Sc. Silvio Parpart</dc:description>
  <dc:description xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Dissertation Universität Rostock 2018</dc:description>
  <dc:subject xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">540</dc:subject>
  <dc:subject xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">547.2</dc:subject>
  <dc:subject xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">540</dc:subject>
  <dc:subject xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">35.69</dc:subject>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">http://rosdok.uni-rostock.de/resolve/urn/urn:nbn:de:gbv:28-diss2018-0094-3</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">https://doi.org/10.18453/rosdok_id00002100</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">https://nbn-resolving.org/urn:nbn:de:gbv:28-diss2018-0094-3</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">https://d-nb.info/1293652814/34</dc:identifier>
  <dc:relation xmlns:dc="http://purl.org/dc/elements/1.1/">Synthese polycyclischer aromatischer Stickstoff-Heterocyclen--(DE-627)1024482448</dc:relation>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">urn:nbn:de:gbv:28-diss2018-0094-3</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">doi: 10.18453/rosdok_id00002100</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">oclc: 1042090865</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">ppn:
				(DE-627)1025300173</dc:identifier>
</oai_dc:dc>
