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a bibo:Issue;
dcterms:medium ;
rdau:P60049 ;
rdau:P60050 ;
rdau:P60048 ;
dc:identifier "(DE-101)132877855X";
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a bibo:Article;
dc:title "Reaktionen enolischer Zuckerderivate, XIV. Eine neue Synthese von l ‐Fucosamin durch „Azidonitratisierung”︁ von l ‐Fucal";
dcterms:creator _:node1jup9asl5x9510433 .
_:node1jup9asl5x9510433 gndo:preferredName "Lehmann, Jochen" .
marcRole:aut _:node1jup9asl5x9510434 .
_:node1jup9asl5x9510434 gndo:preferredName "Lehmann, Jochen" .
marcRole:aut _:node1jup9asl5x9510435 .
_:node1jup9asl5x9510435 gndo:preferredName "Reutter, Werner" .
marcRole:aut _:node1jup9asl5x9510436 .
_:node1jup9asl5x9510436 gndo:preferredName "Schöning, Dietgard" .
bibo:pageStart "1470";
bibo:pageEnd "1472";
dcterms:extent "3 S.";
dcterms:isPartOf ;
dcterms:description "Reactions of Enolic Sugar Derivatives, XIV. A New Synthesis of l‐Fucosamine by „Azido‐nitration”︁ of l‐Fucal Starting from 3,4‐di‐O‐acetyl‐l‐fucal (2) 3,4‐di‐O‐acetyl‐2‐azido‐2‐deoxy‐α‐l‐fucopyranosyl nitrate (3) was prepared by azido‐nitration. Ammonolysis and reacetylation led to 1–N,3,4‐O‐triacetyl‐2‐azido‐2‐deoxy‐α‐l‐fucopyranosylamine (4). De‐O‐acetylated 4 (5) was hydrogenized to yield crude l‐N‐acetyl‐2‐amino‐2‐deoxy‐α‐l‐fucopyranosylamine which after acid hydrolysis yielded l‐fucosamine (1)."@de;
dcterms:license ;
wdrs:describedby .
dcterms:license ;
dcterms:modified "2024-05-09T21:39:56.000"^^xsd:dateTime .
dcterms:issued "2006";
bibo:issue "112.2006, 4";
owl:sameAs .