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<https://d-nb.info/1328838749> 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)1328838749";
  umbel:isLike <https://doi.org/10.1002/cber.19751081106>, <https://nbn-resolving.org/urn:nbn:de:101:1-2405100333413.779103963181>;
  dcterms:format <https://www.iana.org/assignments/media-types/application/pdf>;
  foaf:primaryTopic <https://doi.org/10.1002/cber.19751081106>;
  dcterms:language <http://id.loc.gov/vocabulary/iso639-2/eng>;
  a bibo:Article;
  dc:title "Organische Synthesen im Plasma von Glimmentladungen, XVI †. Ring‐Ketten‐Isomerisierungen an Stickstoffheterocyclen ‡";
  dcterms:creator _:node1jrarau8gx45920823 .

_:node1jrarau8gx45920823 gndo:preferredName "Suhr, Harald" .

<https://d-nb.info/1328838749> marcRole:aut _:node1jrarau8gx45920824 .

_:node1jrarau8gx45920824 gndo:preferredName "Suhr, Harald" .

<https://d-nb.info/1328838749> marcRole:aut _:node1jrarau8gx45920825 .

_:node1jrarau8gx45920825 gndo:preferredName "Schöch, Ursula" .

<https://d-nb.info/1328838749> bibo:pageStart "3469";
  bibo:pageEnd "3474";
  dcterms:extent "6 S.";
  dcterms:isPartOf <https://ld.zdb-services.de/resource/2224932-1>;
  dcterms:description "Organic Syntheses in Glow Discharges, XVI. Ring‐Open Chain Isomerisation of Nitrogen Heterocycles Glow discharges easily convert pyrrol, pyridine, indole, quinoline, and isoquinoline into unsaturated open chain nitriles, which are either condensed in cool traps or form polymers on the walls of the reactor. A similar isomerisation including cleavage of a benzene ring is observed for aniline and 1H‐benzotriazole."@de,
    "Abstract: Im Plasma von Glimmentladungen isomerisieren Stickstoffheterocyclen wie Pyrrol, Pyridin, Indol, Chinolin und Isochinolin sehr leicht zu offenkettigen ungesättigten Nitrilen, die entweder als Substanz oder als Polymerisat (Wandbelag) anfallen. Ring‐Ketten‐Isomerisierungen unter Aufspaltung des aromatischen Ringes wurden bei Anilin und 1H‐Benzotriazol beobachtet."@de;
  dcterms:license <http://onlinelibrary.wiley.com/termsAndConditions#vor>;
  wdrs:describedby <https://d-nb.info/1328838749/about> .

<https://d-nb.info/1328838749/about> dcterms:license <http://creativecommons.org/publicdomain/zero/1.0/>;
  dcterms:modified "2024-05-10T21:43:22.000"^^xsd:dateTime .

<https://d-nb.info/1328838749> dcterms:issued "2006";
  bibo:issue "108.2006, 11";
  owl:sameAs <http://hub.culturegraph.org/resource/DNB-1328838749> .

