<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>Pisella G</dc:creator>
  <dc:creator>Gagnebin A</dc:creator>
  <dc:creator>Waser J</dc:creator>
  <dc:date>2020</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Multicomponent reactions provide efficient means to access molecular complexity. Herein, we report a copper-catalyzed three-component reaction of diazo compounds, alcohols and ethynyl benziodoxole (EBX) reagents for the synthesis of propargyl ethers. Extensive variations of the three partners of the reaction is possible, leading to highly functionalized and structurally diverse products under mild conditions. Alkynylation of a copper ylide intermediate is postulated as key step for this transformation.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/97021</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.202001317</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/32187739</dc:relation>
  <dc:source>Chemistry (Weinheim an der Bergstrasse, Germany). - 2020</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">carbenes</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">copper catalysis</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">hypervalent iodine reagents</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">multi-component reactions (MCR)</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">synthetic methods</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Three-Component Reaction for the Synthesis of Highly Functionalized Propargyl Ethers.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>