<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>Débieux, Jean-Luc</dc:creator>
  <dc:creator>Cosandey, Anne</dc:creator>
  <dc:creator>Helgen, Céline</dc:creator>
  <dc:creator>Bochet, Christian G.</dc:creator>
  <dc:date>2007-01-08</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">We report here conditions which allow the photoacylation of primary, secondary and tertiary alcohols with N-acetyl-5,7-dinitroindoline under exceptionally mild conditions, at wavelengths harmless to most functional groups, including otherwise photosensitive ones.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/unifr/documents/300458</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/300458/files/bochet_pan.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/ejoc.200600790</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>European Journal of Organic Chemistry. - 2007, p. 2073 - 2077</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Alcohols</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Esters</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Acylation</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Protecting groups</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Photochemistry</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Photoacylation of alcohols in neutral medium</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>