Allylation of ketones via their enol acetates catalyzed by palladium-phosphine complexes and organotin compounds

Jiro Tsuji, Ichiro Minami, Isao Shimizu

    Research output: Contribution to journalArticle

    43 Citations (Scopus)

    Abstract

    Enol acetates are converted to allyl ketones by the reaction of allylic carbonates in the presence of palladium-phosphine complex and tin alkoxide as bimetallic catalysts.

    Original languageEnglish
    Pages (from-to)4713-4714
    Number of pages2
    JournalTetrahedron Letters
    Volume24
    Issue number43
    DOIs
    Publication statusPublished - 1983

    Fingerprint

    phosphine
    Organotin Compounds
    Allylation
    Tin
    Carbonates
    Palladium
    Ketones
    Acetates
    Catalysts

    ASJC Scopus subject areas

    • Biochemistry
    • Organic Chemistry
    • Drug Discovery

    Cite this

    Allylation of ketones via their enol acetates catalyzed by palladium-phosphine complexes and organotin compounds. / Tsuji, Jiro; Minami, Ichiro; Shimizu, Isao.

    In: Tetrahedron Letters, Vol. 24, No. 43, 1983, p. 4713-4714.

    Research output: Contribution to journalArticle

    Tsuji, Jiro ; Minami, Ichiro ; Shimizu, Isao. / Allylation of ketones via their enol acetates catalyzed by palladium-phosphine complexes and organotin compounds. In: Tetrahedron Letters. 1983 ; Vol. 24, No. 43. pp. 4713-4714.
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    abstract = "Enol acetates are converted to allyl ketones by the reaction of allylic carbonates in the presence of palladium-phosphine complex and tin alkoxide as bimetallic catalysts.",
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