<?xml version="1.0" encoding="UTF-8"?>
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  <identifier identifierType="DOI">10.18453/rosdok_id00001646</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Gevorgyan, Ashot</creatorName>
      <givenName>Ashot</givenName>
      <familyName>Gevorgyan</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1079688854</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Exploration of transition-metal-catalyzed direct C-H arylation of nitro-substituted heteroarenes and further transformations of nitro group</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2015</publicationYear>
  <resourceType resourceTypeGeneral="Text" />
  <subjects>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">540 Chemistry &amp; allied sciences</subject>
  </subjects>
  <dates>
    <date dateType="Created">2015</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00001646</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2015-0196-5</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">The present work aimed to study the transition-metal-catalyzed direct C-H arylation of various nitro-substituted heteroarenes, including 4-nitroimidazole derivatives, 4-nitropyrazole derivatives, fused 3-nitropyridines, nitro-substituted pyrrole and thiophene. Under optimized reaction conditions a wide range of coupling partners were perfectly tolerated. Additional empirical studies indicated that the nitro group has influence on the regioselectivity of the reactions. In addition, the multipurpose nature of nitro group as a versatile directing group was explored.</description>
  </descriptions>
</resource>
