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<https://d-nb.info/1328854485> a bibo:Issue;
  dcterms:medium <http://rdaregistry.info/termList/RDACarrierType/1018>;
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  rdau:P60048 <http://rdaregistry.info/termList/RDACarrierType/1018>;
  dc:identifier "(DE-101)1328854485";
  umbel:isLike <https://doi.org/10.1002/cber.19751080719>, <https://nbn-resolving.org/urn:nbn:de:101:1-2405100653189.320127021966>;
  dcterms:format <https://www.iana.org/assignments/media-types/application/pdf>;
  foaf:primaryTopic <https://doi.org/10.1002/cber.19751080719>;
  dcterms:language <http://id.loc.gov/vocabulary/iso639-2/eng>;
  a bibo:Article;
  dc:title "1‐Amino‐2,6‐hexacosamethylen‐4‐pyridon, eine Ausgangsverbindung für eine mögliche Catenan‐Synthese";
  dcterms:creator _:node1k0rmm5k0x23704830 .

_:node1k0rmm5k0x23704830 gndo:preferredName "Isele, Gerand L." .

<https://d-nb.info/1328854485> marcRole:aut _:node1k0rmm5k0x23704831 .

_:node1k0rmm5k0x23704831 gndo:preferredName "Isele, Gerand L." .

<https://d-nb.info/1328854485> marcRole:aut _:node1k0rmm5k0x23704832 .

_:node1k0rmm5k0x23704832 gndo:preferredName "Scheib, Klaus" .

<https://d-nb.info/1328854485> bibo:pageStart "2312";
  bibo:pageEnd "2319";
  dcterms:extent "8 S.";
  dcterms:isPartOf <https://ld.zdb-services.de/resource/2224932-1>;
  dcterms:description "1‐Amino‐2,6‐hexacosamethylen‐4‐pyridon, a Potential Starting Compound for the Synthesis of a Catenane Four synthetic pathways to the 2,6‐disubstituted 1‐amino‐4‐pyridone 16 from 9,12‐heneicosa‐diyne‐11‐one (10) are described. The synthesis of the title compound 22 is performed by cyclisation of 2,6‐di (12‐tridecynyl)‐4‐pyridone (19c), followed by catalytic hydrogenation of the triple bonds and N‐amination with chloroamine/sodium hydride in DMF. O‐Amino‐4‐pyridones (17, 23) are formed as by‐products during this procedure."@de,
    "Abstract: Vier Synthesewege für das 2,6‐disubstituierte 1‐Amino‐4‐pyridon 16 aus 9,12‐Heneicosadiin‐11‐on (10) werden beschrieben. Die Titelverbindung 22 wird dargestellt durch Cyclisierung von 2,6‐Di‐(12‐tridecinyl)‐4‐pyridon (19c), katalytische Hydrierung der Dreifachbindungen und N‐Aminie‐rung mit Chloramin/Natriumhydrid in Dimethylformamid. Als Nebenprodukte bilden sich bei diesem Verfahren O‐Amino‐4‐pyridone (17, 23)."@de;
  dcterms:license <http://onlinelibrary.wiley.com/termsAndConditions#vor>;
  wdrs:describedby <https://d-nb.info/1328854485/about> .

<https://d-nb.info/1328854485/about> dcterms:license <http://creativecommons.org/publicdomain/zero/1.0/>;
  dcterms:modified "2024-05-10T21:45:12.000"^^xsd:dateTime .

<https://d-nb.info/1328854485> dcterms:issued "2006";
  bibo:issue "108.2006, 7";
  owl:sameAs <http://hub.culturegraph.org/resource/DNB-1328854485> .

