ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Collection
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 423-426 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Rel. Configuration and Crystal Structure of a Bufadienolide AnalogueThe X-ray analysis of 4 surprisingly proved a cis substitution pattern within the five-membered ring. Furthermore a conformational similarity between 3 and 4 is shown.
    Notes: Die Röntgenstrukturanalyse am Perhydrostilben-α-Pyron 4 bringt den überraschenden Befund einer cis-Anordnung der Substituenten im Cyclopentanring. Im übrigen entspricht die Konformation des Moleküls weitgehend der Verbindung 3.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Unsaturated Lactones with Steroidal-Type Skeleton, VIII. - Synthesis of 4-Substituted Ethyl 4,5-Epoxy-trans-2-pentenoates and Their Cyclization to α-PyronesThe bufadienolide 4 has been synthesized in high yield for pharmacological screening. The previously described acid 5 a has been transformed via 6 → 7 → 8 → 9 into the aldehyde 10. Aldol reaction provided access to 11 which in turn afforded 15 on epoxidation and Horner olefination. In spite of the trans-configuration of the C=C bond 15 has been cyclized by a novel one-step method to the α-pyrone 16 which was easily converted into 4.
    Notes: Für die pharmakologische Prüfung wurde das Bufadienolid 4 mit hoher Ausbeute synthetisiert. Die früher beschriebene Carbonsäure 5 a ließ sich über 6 → 7 → 8 → 9 in den Aldehyd 10 überführen. Nach Aldolkondensation lieferte dieser 11, aus dem mittels Epoxidierung und Horner-Olefinierung 15 resultierte. Trotz trans-Konfiguration der C=C-Bindung ließ sich 15 in einem Schritt nach einem neuartigen Verfahren zum α-Pyron 16 cyclisieren, das leicht in 4 umgewandelt werden konnte.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...