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  • 1
    Electronic Resource
    Electronic Resource
    The Formal Total Synthesis of Epothilone A (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2817-2823 
    Details
    ISSN: 1434-193X
    Keywords: Epothilone A ; Ring-closing metathesis ; Aldol reactions ; Lactones ; Diastereoselective alkylation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formal total synthesis of epothilone A is described. The key steps in the synthesis of the northern hemisphere are a Z-selective ten-membered ring-closing metathesis reaction (RCM) and the diastereoselective alkylation at C8. Aldehyde 3 is formed by introduction of the thiazole moiety by a Wittig reaction and subsequent functional group transformation. An efficient route to keto acid 5 is described.
    Type of Medium: Electronic Resource
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