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Synthesis of beta-chloro-alpha-aminophosphonate derivatives via the regioselective ring opening of unactivated aziridine-2-phosphonates

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


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{
  "@context": "https://schema.org/", 
  "@id": 33007, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Canakkale Onsekiz Mart Univ, Dept Chem Engn, Canakkale, Turkey", 
      "name": "Polat-Cakir, Sidika"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Middle East Tech Univ, Dept Chem, Ankara, Turkey", 
      "name": "Beksultanova, Nurzhan"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Middle East Tech Univ, Dept Chem, Ankara, Turkey", 
      "name": "Dogan, Ozdemir"
    }
  ], 
  "datePublished": "2018-01-01", 
  "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.", 
  "headline": "Synthesis of beta-chloro-alpha-aminophosphonate derivatives via the regioselective ring opening of unactivated aziridine-2-phosphonates", 
  "identifier": 33007, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "Synthesis of beta-chloro-alpha-aminophosphonate derivatives via the regioselective ring opening of unactivated aziridine-2-phosphonates", 
  "url": "https://aperta.ulakbim.gov.tr/record/33007"
}
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