1 Ocak 2019 Dergi makalesi Açık Erişim

Sendil, Kivilcim; Keskin, Selbi; Balci, Metin

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  <dc:creator>Sendil, Kivilcim</dc:creator>
  <dc:creator>Keskin, Selbi</dc:creator>
  <dc:creator>Balci, Metin</dc:creator>
  <dc:date>2019-01-01</dc:date>
  <dc:description>A concise and regioselective approach to the synthesis of pyridine-fused heterocycles and benzoxazepine derivatives was developed. Propargyl imines derived from aromatic aldehydes and propargyl amine underwent 6 pi-electrocyclization reactions at high temperatures in high yields to form pyridine-fused heterocycles. Application of the same methodology to aromatic imines having a hydroxyl group in the ortho position resulted in the formation of (benz)oxazepine derivatives. The formation mechanism of the products was discussed. (C) 2019 Elsevier Ltd. All rights reserved.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/74961</dc:identifier>
  <dc:identifier>oai:zenodo.org:74961</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 75(46)</dc:source>
  <dc:title>Concise design and synthesis of pyridine-fused heterocycles via 6 pi- Azaelectrocyclization process of iminoalkyne derivatives</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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