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B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans.

B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans. Research Abstract Details 

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  • B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans. Abstract Text:

    Unprotected homoallylic alcohols can be directly converted to cis-2,6-disubstituted pyrans by palladium catalyzed B-alkyl Suzuki coupling and subsequent Michael addition.

    B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans. Publishing Authors By Initials

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    B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Chemical communications (Cambridge, England)

    VOLUME:

    Page Numbers: 4294-6

    Journal Abbreviation: Chem. Commun. (Camb.)

    ISSN: 1359-7345

    DAY: 16

    MONTH: 07

    YEAR: 2008

    B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans. Information

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    LANGUAGE: eng

    NlmUniqueID: 9610838

    B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans. Keywords Mesh Terms:

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    Grant and Affiliation Information for B-Alkyl Suzuki couplings for the stereoselective synthesis of substituted pyrans.

    AFFILIATION: Max-Planck-Institut für Kohlenforschung, D-45470, Mülheim/Ruhr, Germany. fuerstner@mpi-muelheim.mpg.de.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Chem Commun (Camb)

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