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<https://d-nb.info/1328970736> a bibo:Issue;
  dcterms:medium <http://rdaregistry.info/termList/RDACarrierType/1018>;
  rdau:P60049 <http://rdaregistry.info/termList/RDAContentType/1020>;
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  rdau:P60048 <http://rdaregistry.info/termList/RDACarrierType/1018>;
  dc:identifier "(DE-101)1328970736";
  umbel:isLike <https://doi.org/10.1002/cber.19761090601>, <https://nbn-resolving.org/urn:nbn:de:101:1-2405110556523.256581679355>;
  dcterms:format <https://www.iana.org/assignments/media-types/application/pdf>;
  foaf:primaryTopic <https://doi.org/10.1002/cber.19761090601>;
  dcterms:language <http://id.loc.gov/vocabulary/iso639-2/eng>;
  a bibo:Article;
  dc:title "Untersuchung chromatographischer Racemattrennungen, VI. Polymere Aminosäurederivate als optisch aktive Adsorbentien";
  dcterms:creator _:node1jrf5vkmpx43772653 .

_:node1jrf5vkmpx43772653 gndo:preferredName "Blaschke, Gottfried" .

<https://d-nb.info/1328970736> marcRole:aut _:node1jrf5vkmpx43772654 .

_:node1jrf5vkmpx43772654 gndo:preferredName "Blaschke, Gottfried" .

<https://d-nb.info/1328970736> marcRole:aut _:node1jrf5vkmpx43772655 .

_:node1jrf5vkmpx43772655 gndo:preferredName "Schwanghart, Anne‐Dore" .

<https://d-nb.info/1328970736> bibo:pageStart "1967";
  bibo:pageEnd "1975";
  dcterms:extent "9 S.";
  dcterms:isPartOf <https://ld.zdb-services.de/resource/2224932-1>;
  dcterms:description "Investigation of Chromatographic Resolutions of Racemates, VI. Polymeric Amino Acid Derivatives as Optically Active Adsorbens Starting with optically active amino acids, the polyacrylamides 3a–h, 5a–d and 6a, b the polymethacrylamides 8a–c and the polyacrylic ester 6f were synthesized. The separation efficiencies of these polymers were determined by chromatography of racemic mandelic acid and mandelamide, respectively. The best separations of the enantiomers of both racemates were observed on the phenylalanine derivatives 3e and 5a."@de,
    "Abstract: Die Polyacrylamide 3a–h, 5a–d und 6a, b die Polymethacrylamide 8a–c und der Polyacrylsäureester 6f wurden aus optisch aktiven Aminosäurederivaten hergestellt und auf ihre Trennwirkung durch Chromatographie racem. Mandelsäure sowie racem. Mandelamids geprüft. Die beste Trennung der Enantiomeren beider Racemate wurde an den Phenylalaninderivaten 3e und 5a beobachtet."@de;
  dcterms:license <http://onlinelibrary.wiley.com/termsAndConditions#vor>;
  wdrs:describedby <https://d-nb.info/1328970736/about> .

<https://d-nb.info/1328970736/about> dcterms:license <http://creativecommons.org/publicdomain/zero/1.0/>;
  dcterms:modified "2024-05-13T18:26:24.000"^^xsd:dateTime .

<https://d-nb.info/1328970736> dcterms:issued "2006";
  bibo:issue "109.2006, 6";
  owl:sameAs <http://hub.culturegraph.org/resource/DNB-1328970736> .

