<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>Wang Q</dc:creator>
  <dc:creator>Zhu J</dc:creator>
  <dc:date>2011</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Macrocyclization methodologies allowing access to macrocycles having an endo aryl ether and an endo aryl-aryl bond, especially those based on an intramolecular S(N)Ar reaction and the Suzuki-Miyaura reaction, are summarized. Total synthesis of complestatin, a bis-macrocyclic natural product, featuring these two technologies are presented.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/176857</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.2533/chimia.2011.168</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/21528652</dc:relation>
  <dc:source>Chimia. - 2011</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Catalysis</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Chlorophenols</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Complement Pathway, Alternative</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Ethers</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Heterocyclic Compounds</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Peptides, Cyclic</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Access to macrocycles with an endo aryl ether and an endo aryl-aryl bond, development and application.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>