<?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">3-substituted chromones as convenient building blocks for the design and synthesis of functionalized 2-hydroxybenzophenones, 6H-benzo[c]chromenes, benzo[c]coumarins, fused pyridine derivatives, 2-salicyloylfurans and 2-benzoyl-8H-thieno[2,3-b]indoles</dc:title>
  <dc:title xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Three-substituted</dc:title>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Savych, Iryna , 1988- (VerfasserIn)</dc:contributor>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Langer, Peter , 1969- (GutachterIn)</dc:contributor>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Müller, Thomas J. J. (GutachterIn)</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">2014</dc:date>
  <dc:date xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">2014</dc:date>
  <dc:language xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">eng</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">The present thesis is dedicated to the study of synthetic potential of 3-substituted chromones, namely 3-acyl- and 3-halochromones, illustrated by regioselective cyclocondensation reactions with different binucleophiles and describes the design and synthesis of novel biologically relevant carbo- and heterocycles. Various fluorine-containing products were synthesized using 3-perfluoroacylchromones. In addition, new promising candidates for UV-A/B filters and fluorescent compounds have been synthesized and analyzed.&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">Die vorliegende Arbeit beschreibt das synthetische Potential von 3-Substituierten Chromonen, nämlich 3-Acyl- und 3-Halogenchromonen, durch Dominoreaktionen mit verschiedenen Dinukleophilien und ist dem Design und der Synthese von neuartigen biologisch relevanten Carbo- und Heterocyclen gewidmet. Verschiedene fluorierte Produkte wurden durch den Gebrauch von 3-Fluoroacylchromonen hergestellt. Einige synthetisierte Substanzen zeigen vielversprechende Absorption- und Fluoreszenzeigenschaften.&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">vorgelegt von Iryna Savych</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 2015</dc:description>
  <dc:subject xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">547.59</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">35.50</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-diss2016-0059-8</dc:identifier>
  <dc:relation xmlns:dc="http://purl.org/dc/elements/1.1/">3-substituted chromones as convenient building blocks for the design and synthesis of functionalized 2-hydroxybenzophenones, 6H-benzo[c]chromenes, benzo[c]coumarins, fused pyridine derivatives, 2-salicyloylfurans and 2-benzoyl-8H-thieno[2,3-b]indoles--(DE-627)826609953</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-diss2016-0059-8</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">oclc: 952471496</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">ppn:
				(DE-627)862229391</dc:identifier>
</oai_dc:dc>
