<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>Gautschi D</dc:creator>
  <dc:creator>Leumann CJ</dc:creator>
  <dc:date>2003</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The olefinic peptide nucleic acid analogues (OPA) monomers containing the bases thymine and adenine were synthesised in 11 steps. Fully modified oligomers containing these units were prepared and their pairing properties assessed by means of UV-melting experiments.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/182748</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1081/NCN-120022838</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/14565382</dc:relation>
  <dc:source>Nucleosides, nucleotides &amp; nucleic acids. - 2003</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Adenine</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Alkenes</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Base Pairing</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Base Sequence</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Mass Spectrometry</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Nucleic Acid Denaturation</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Oligodeoxyribonucleotides</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Peptide Nucleic Acids</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Thymine</dc:subject>
  <dc:title xmlns:ns10="xml" ns10:lang="en">Olefinic peptide nucleic acid (OPA).</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>