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Asymmetric total synthesis of (+)-phoslactomycin B.

Asymmetric total synthesis of (+)-phoslactomycin B. Research Abstract Details 

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  • Asymmetric total synthesis of (+)-phoslactomycin B. Abstract Text:

    (+)-Phoslactomycin B was synthesized by a highly enantio- and stereoselective approach involving asymmetric pentenylation, Suzuki-Miyaura coupling, ring-closing metathesis, asymmetric dihydroxylation, and Stille coupling. The synthetic method developed enables us to synthesize three other isomers concerning the C11-OH and Delta (12)-double bond.

    Asymmetric total synthesis of (+)-phoslactomycin B. Publishing Authors By Initials

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    MEDLINE DATE:

    Asymmetric total synthesis of (+)-phoslactomycin B. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Organic letters

    VOLUME: 10

    Page Numbers: 2139-42

    Journal Abbreviation: Org. Lett.

    ISSN: 1523-7060

    DAY: 8

    MONTH: 05

    YEAR: 2008

    Asymmetric total synthesis of (+)-phoslactomycin B. Information

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    LANGUAGE: eng

    NlmUniqueID: 100890393

    Asymmetric total synthesis of (+)-phoslactomycin B. Keywords Mesh Terms:

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    Grant and Affiliation Information for Asymmetric total synthesis of (+)-phoslactomycin B.

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    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Org Lett

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