<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" 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:creator>Zysman-Colman, Eli</dc:creator>
  <dc:creator>Arias, Karla</dc:creator>
  <dc:creator>Siegel, Jay S.</dc:creator>
  <dc:description xmlns:ns0="xml" ns0:lang="en">&lt;jats:p&gt; Regioselective and chemoselective electrophilic bromination of a wide series of activated arenes using N-bromosuccinimide (NBS) in acetonitrile occurs readily. Environmentally friendly conditions, large substrate scope, and ease of synthesis enhance the utility of this method over other electrophilic bromination conditions. &lt;/jats:p&gt;</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/82213</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1139/v08-176</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/issn/0008-4042</dc:relation>
  <dc:source>Canadian Journal of Chemistry. - Canadian Science Publishing. - 2009, vol. 87, no. 2, p. 440-447</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Organic Chemistry</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">General Chemistry</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Catalysis</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Synthesis of arylbromides from arenes and N-bromosuccinimide (NBS) in acetonitrile — A convenient method for aromatic bromination</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>