1 Ocak 2016 Dergi makalesi Açık Erişim

Kazancioglu, Mustafa Zahrittin; Kazancioglu, Elif Akin; Secen, Hasan; Altundas, Ramazan

Dublin Core

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  <dc:creator>Kazancioglu, Mustafa Zahrittin</dc:creator>
  <dc:creator>Kazancioglu, Elif Akin</dc:creator>
  <dc:creator>Secen, Hasan</dc:creator>
  <dc:creator>Altundas, Ramazan</dc:creator>
  <dc:date>2016-01-01</dc:date>
  <dc:description>The oxidation reactions of various azidoalkyl furans were explored under different conditions to access structurally complex compounds from simple starting materials in an operationally simple, single step reaction. The strategically placed azide functional groups on the alkyl chain of the furan led to the discovery of a new and simple method for the synthesis of five-, six-, and seven-membered nitrogen heterocycles bearing prochiral centers and stereocenters. (C) 2016 Elsevier Ltd. All rights reserved.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/55655</dc:identifier>
  <dc:identifier>oai:zenodo.org:55655</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>TETRAHEDRON LETTERS 57(50) 5611-5615</dc:source>
  <dc:title>Oxidation of azidoalkyl furans</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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