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  • 1960-1964  (3)
  • 1955-1959  (1)
  • 1960  (3)
  • 1959  (1)
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  • 1960-1964  (3)
  • 1955-1959  (1)
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Keywords
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 713-717 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: With alkylbenzylamine D-glucose undergoes AMADORI-rearrangement to 1-alkyl-benzylamino-1-deoxy-D-fructose. Catalytic hydrogenolysis of the benzyl group gives rise to 1-alkylamino-1-deoxy-D-fructose (alkyl-fructosamine). In this way, the methyl, ethyl and butyl derivatives of fructosamine have been prepared in crystalline form. With isocyanic acid and rhodanic acid the 1-alkylamino-1-deoxy-D-fructoses are converted into imidazole derivatives, as expected for substances of the α-aminoketone type.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 42 (1959), S. 2447-2451 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Synthese von 3,6-Didesoxy-3-amino-D-altrose-hydrochlorid wird beschrieben. Die Isomerisierung der 3-Amino-3-desoxy-D-methylaltrosid-Derivate unter hydrolytischen Bedingungen wird durch die Annahme semisesselförmiger Ionenpaare als Zwischenzustände erklärt.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 1787-1795 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of isocyanic acid and of thiocyanic acid with the products of AMADORI rearrangements are described. Thiocyanic acid, especially, is well suited for the characterization of fructosamines. By etherification of the mercapto group and exposure to oxidizing agents, the 2-mercapto-imidazoles can be used for preparation of certain imidazole derivatives which are otherwise difficult to obtain, e.g. 4-formyl-imidazole.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 129-135 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Epoxydöffnungen an Pyranose-Ringen wurden konformationsanalytisch untersucht. Den Epoxyden wird Semisesselkonformation zugeschrieben. Die meisten experimentellen Ergebnisse der Literatur bestätigen die Annahme, dass der Angriff axial erfolgt und dass im Laufe der Substitutionsreaktion keine Konformations-änderung stattfindet.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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