<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>Germain N</dc:creator>
  <dc:creator>Schlaefli D</dc:creator>
  <dc:creator>Chellat M</dc:creator>
  <dc:creator>Rosset S</dc:creator>
  <dc:creator>Alexakis A</dc:creator>
  <dc:date>2014</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Enantioenriched Al-, Mg-, and Zn-enolates undergo electrophilic trapping by nitroolefins and vinylsulfones to afford 1,4-diketones and 2-(bis(phenylsulfonyl)ethyl)ketones in good yield and excellent diastereoselectivity. A one-pot preparation of indenes and enantiopure syntheses of tetrahydrobenzofurans, tetrahydrobenzopyrroles, and azulenes are disclosed. A site-selective two-step sequence of three conjugate additions is also demonstrated.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/106392</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/ol5005752</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/24661026</dc:relation>
  <dc:source>Organic letters. - 2014</dc:source>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Domino asymmetric conjugate addition-conjugate addition.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>