1 Ocak 2018 Dergi makalesi Açık Erişim

Polat-Cakir, Sidika; Beksultanova, Nurzhan; Dogan, Ozdemir

Dublin Core

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  <dc:creator>Polat-Cakir, Sidika</dc:creator>
  <dc:creator>Beksultanova, Nurzhan</dc:creator>
  <dc:creator>Dogan, Ozdemir</dc:creator>
  <dc:date>2018-01-01</dc:date>
  <dc:description>A series of unactivated racemic and chiral aziridine-2-phosphonates were synthesized by modified Gabriel-Cromwell reaction. Ring opening reaction of the synthesized phosphonates by gaseous HCl provided access to a wide range of biologically interesting novel beta-chloro-alpha-aminophosphonates. All reactions toward each of the above-mentioned products can be conducted regioselectively in high yields.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/33007</dc:identifier>
  <dc:identifier>oai:zenodo.org:33007</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS 193(12) 858-864</dc:source>
  <dc:title>Synthesis of beta-chloro-alpha-aminophosphonate derivatives via the regioselective ring opening of unactivated aziridine-2-phosphonates</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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