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  • Articles  (2)
  • Organic Chemistry  (2)
  • 2015-2019
  • 1985-1989  (1)
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  • 1955-1959
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1985 (1985), S. 644-649 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical Modification of Kanamycin A. - Derivatives Containing a 4,5-Double Bond in the Kanosamine PartOxidation of the primary alcohol group in the kanamycin A derivative 2b with simultaneous β-elimination gave the α,β-unsaturated aldehyde 3a of which the derivatives 3b - e were prepared by acetalisation, oxidation, or reduction. Hydrogenation of the double bond led to 4 ‚-deoxy-5‘-epi-kanamycin A derivatives.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of D-Glucuronic Acid, X.  -  Elimination Reactions of D-Glucofuranurono-6,3-lactone and its DerivativesIn the presence of bases D-glucofuranurono-6,3-lactone, its glycosides, and their 2,5-di-O-alkyl derivatives, respectively, form doubly unsaturated products. This reaction is initiated by proton abstraction at C-5 causing β-elimination with opening of the tetrahydrofuran ring and liberation of the aldehyde function. In a subsequent second elimination (2E, 4Z)-2,5-dihydroxy-and (2E, 4Z)-2,5-dialkoxy-6-oxo-2,4-hexadienoic acid, respectively, are formed, of which the former spontaneously isomerizes to the thermodynamically more stable (2Z, 4Z)-conformer.
    Notes: D-Glucofuranurono-6,3-lacton, seine Glykoside und deren 2,5-Di-O-alkylderivate reagieren mit Basen unter Bildung doppelt ungesättigter Produkte. Diese Reaktion wird durch Protonabstraktion an C-5 eingeleitet, wobei der Tetrahydrofuranring durch β-Eliminierung geöffnet und die Aldehydgruppe in Freiheit gesetzt wird. In der daran anschließenden Aldoleliminierung bilden sich (2E, 4Z)-2,5-Dihydroxy-oder (2E, 4Z)-2,5-Dialkoxy-6-oxo-2,4-hexadiensäure, von denen die erstere spontan zum thermodynamisch stabileren (2Z, 4Z)-Konformeren isomeriiert.
    Type of Medium: Electronic Resource
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