1 Ocak 2015 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>2015-01-01</dc:date>
  <dc:description>The oxidation reactions of amino and hydroxylamino substituted alkylfurans were explored for the synthesis of structurally complex compounds from simple starting materials. A novel photooxygenation of the furan derivatives gave an alpha,beta-unsaturated dicarbonyl moiety which underwent subsequent conjugate addition to yield diastereomeric mixtures of the corresponding pyrrolidine and isoxazoline heterocycles. Oxidation of the alpha,beta-unsaturated dicarbonyl using mCPBA gave epoxide intermediates, which were opened by nucleophilic attack of the amino groups, furnishing pyrrolidine and isoxazolidine heterocycles. (C) 2015 Elsevier Ltd. All rights reserved.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/82287</dc:identifier>
  <dc:identifier>oai:zenodo.org:82287</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 56(50) 6994-6997</dc:source>
  <dc:title>Oxidation of aminoalkyl and hydroxylaminoalkyl furans</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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