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  • 1
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of rac-Stercobilin IX α with the Configuration of the Natural Product and of Some Urobilins, Half-stercobilins, and Stercobilins with Unequivocal Constitution and configurationFor the first time a stercobilin IX α (12) with the configuration of the natural product and some half-stercobilins, e. g. 9, with the same configuration were synthesized. In addition some bile pigments of the urobilin - half-stercobilin and stercobilin type with determined configuration were prepared.
    Notes: Erstmals wurden ein Stercobilin IX α (12) mit der relativen Konfiguration des Naturproduktes und eine Reihe von Halbstercobilinen, z. B. 9, mit der gleichen Konfiguration dargestellt. Außerdem wurden einige Gallenfarbstoffe der Urobilin - Halbstercobilin- und Stercobilin-Reihe mit definierter Konfiguration synthetisiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1984 (1984), S. 1441-1453 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of Stereoisomeric 3,4-Dihydrobilirubinic Acid Derivatives as Building Blocks for the Synthesis of Bile PigmentsBy reduction of 5′-carboxyneoxanthobilirubinic acid 3 with sodium amalgam in hot water the stereoisomeric 5′-carboxy-3,4-dihydrobilirubinic acids 9 and 15 are formed and from the isomer 4 the stereoisomers 10 and 16 can be obtained. The stereoisomers can be separated by preparative HPLC on reversed-phase silica gel. The unequivocal determination of the configuration was performed with the aldehydes 11, 12 and 17, 18.
    Notes: Durch Reduktion der 5′-Carboxyneoxanthobilirubinsäure 3 mit Natriumamalgam in heißem Wasser gewinnt man die stereoisomeren 5′-Carboxy-3,4-dihydroneobilirubinsäuren 9 und 15 und aus dem Isomeren 4 entsprechend die Stereoisomeren 10 und 16. Die Stereoisomeren lassen sich durch präparative HPLC an Reversed-Phase-Kieselgel voneinander trennen. Die eindeutige sterische Zuordnung erfolgt bei den Aldehyden 11, 12 und 17, 18.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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