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    Unsaturated Fatty Acid Esters Metathesis Catalyzed by Silica Supported WMe5

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    Type
    Article
    Authors
    Riache, Nassima
    Callens, Emmanuel cc
    Talbi, Karima
    Basset, Jean-Marie cc
    KAUST Department
    Chemical Science Program
    Competitive Research Funds
    KAUST Catalysis Center (KCC)
    OCRF- Special Academic Partnership
    Date
    2015-11-14
    Online Publication Date
    2015-11-14
    Print Publication Date
    2016-01
    Permanent link to this record
    http://hdl.handle.net/10754/582471
    
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    Abstract
    Metathesis of unsaturated fatty acid esters (FAEs) by silica supported multifunctional W-based catalyst is disclosed. This transformation represents a novel route towards unsaturated di-esters. Especially, the self-metathesis of ethyl undecylenate results almost exclusively on the homo-coupling product whereas with such catalyst, 1-decene gives ISOMET (isomerization and metathesis olefin) products. The olefin metathesis in the presence of esters is very selective without any secondary cross-metathesis products demonstrating that a high selective olefin metathesis could operate at 150 °C. Additionally, a cross-metathesis of unsaturated FAEs and α-olefins allowed the synthesis of the corresponding ester with longer hydrocarbon skeleton without isomerisation.
    Citation
    Unsaturated Fatty Acid Esters Metathesis Catalyzed by Silica Supported WMe5 2015 Journal of Molecular Catalysis A: Chemical
    Publisher
    Elsevier BV
    Journal
    Journal of Molecular Catalysis A: Chemical
    DOI
    10.1016/j.molcata.2015.11.003
    Additional Links
    http://linkinghub.elsevier.com/retrieve/pii/S1381116915301436
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.molcata.2015.11.003
    Scopus Count
    Collections
    Articles; Chemical Science Program; KAUST Catalysis Center (KCC)

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