<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>Mañas, Carles Giró</dc:creator>
  <dc:creator>Paddock, Victoria L.</dc:creator>
  <dc:creator>Bochet, Christian G.</dc:creator>
  <dc:creator>Spivey, Alan C.</dc:creator>
  <dc:creator>White, Andrew J. P.</dc:creator>
  <dc:creator>Mann, Inderjit</dc:creator>
  <dc:creator>Oppolzer, Wolfgang</dc:creator>
  <dc:date>2010-03-17</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">A fully diastereoselective total synthesis of the lycorenine-type Amaryllidaceae alkaloid (±)-clivonine is reported via a route that employs for the first time a biomimetic ring-switch from a lycorine-type progenitor, thereby corroborating experimentally the biogenetic hypothesis first expounded for these compounds by Barton in 1960.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/301720</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/301720/files/boc_tsl.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/ja910184j</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Journal of the American Chemical Society. - 2010, vol. 132, no. 14, p. 5176–5178</dc:source>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Total synthesis of the lycorenine-type amaryllidaceae alkaloid (±)-clivonine via a biomimetic ring-switch from a lycorine-type progenitor</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>