ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1974 (1974), S. 853-863 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of Moenocinol, the Lipid Part of MoenomycinThe synthesis of moenocinol (1) was achieved from homogeranic acid derivatives 2g or 2h, 4-chloro-2,2-dimethylbutanal (3) and cis-6-chloro-3-methyl-2-hexenyl-tetrahydropyranyl ether (cis-4b). The combination of the synthetic elements cis-4b and 3 proceeded stereospecifically via 5b to give the c-2,t-6-decadiene derivative 6b. The alcohol 1 was synthesised from 6b in three further steps. The identity of the synthetic moenocinol with the genuine lipid was established by spectroscopy. The cis-Δ2-configuration has been directly demonstrated for both compounds by 1H-NMR measurements with Eu(tmhd)3***).
    Notes: Moenocinol (1) wurde aus den Homogeraniumsäurederivaten 2g oder 2h, aus 4-Chlor-2,2-dimethylbutanal (3) sowie cis-6-Chlor-3-methyl-2-hexenyl-tetrahydropyranyläther (cis-4b) aufgebaut. Die Verknüpfung von cis-4b mit 3 führte stereospezifisch über 5b zum c-2,t-6-Decadienderivat 6b, aus dem man in drei weiteren Reaktionsschritten den Alkohol 1 erhielt. Die Identität von synthetischem mit genuinem 1 wurde spektroskopisch bewiesen. Die cis-Δ2-Konfiguration konnte direkt durch 1H-NMR-Messungen mit Eu(tmhd)3***)bewiesen werden.
    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...