1 Ocak 2018 Dergi makalesi Açık Erişim

Cakmak, Osman; Okten, Salih; Alimli, Dilek; Saddiqa, Aisha; Ersanli, Cem Cuneyt

Dublin Core

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  <dc:creator>Cakmak, Osman</dc:creator>
  <dc:creator>Okten, Salih</dc:creator>
  <dc:creator>Alimli, Dilek</dc:creator>
  <dc:creator>Saddiqa, Aisha</dc:creator>
  <dc:creator>Ersanli, Cem Cuneyt</dc:creator>
  <dc:date>2018-01-01</dc:date>
  <dc:description>Quinoline forms the key skeletal component of a number of important natural products and pharmacologically-active compounds. Despite a tremendous amount of research pertaining to the derivatization of quinoline, very few general synthetic routes are described in the literature starting from quinoline or tetrahydroquinoline. A simple and convenient method for the polyfunctionalization of quinolines via nitration of bromoquinolines has been developed. This method represents a new synthetic approach to convert brominated nitroquinoline derivatives into useful cyclic amines via nucleophilic-substitution (SNAr) reaction.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/33959</dc:identifier>
  <dc:identifier>oai:zenodo.org:33959</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>ARKIVOC 362-374</dc:source>
  <dc:title>Activation of 6-bromoquinoline by nitration: synthesis of morpholinyl and piperazinyl quinolines</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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