<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>Bochet, Christian G.</dc:creator>
  <dc:date>2006</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The photochemical liberation of functional groups is an attractive alternative to the  traditional chemical approach. Several photolabile protecting groups have been  developed in the past decades, but they were mainly designed to protect amines and  carboxylic acids. In this account, we present some of our recent work on the  photochemical release of other functions, such as silanols, aldehydes, and ketones.  We also describe a new form of differentiation among several photolabile groups by  the use of monochromatic light tuned to each of them: the chromatic orthogonality.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/300144</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/300144/files/pac200678020241.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1351/pac200678020241</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Pure and Applied Chemistry. - 2006, vol. 78, no. 2, p. 241-247</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Photochemistry</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Protecting groups</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Chromatic orthogonality</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Photochemical release of various functional groups</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
