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De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates.

De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Research Abstract Details 

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  • De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Abstract Text:

    matthew s mortensenMatthew S Mortensen,joshua m osbournJoshua M Osbourn,george a o'dohertyGeorge A O'Doherty,

    A de novo approach to the formal total synthesis of the macrolide natural product (-)-virginiamycin M2 has been achieved via a convergent approach. The absolute and relative stereochemistry of the nonpeptide portion of (-)-virginiamycin M2 was introduced by two Sharpless asymmetric dihydroxylation reactions.

    De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Publishing Authors By Initials

    ms mortensenMS Mortensen,jm osbournJM Osbourn,ga o'dohertyGA O'Doherty,

    For similar polycyclic compounds: macrocyclic compounds: peptides, cyclic: streptogramins: virginiamycin research abstracts see: polycyclic compounds: macrocyclic compounds: peptides, cyclic: streptogramins: virginiamycin research

    PUBMED ID PMID:

    MEDLINE DATE:

    De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Organic letters

    VOLUME: 9

    Page Numbers: 3105-8

    Journal Abbreviation: Org. Lett.

    ISSN: 1523-7060

    DAY: 3

    MONTH: 07

    YEAR: 2007

    De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100890393

    De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Keywords Mesh Terms:

    KEYWORDS: Virginiamycin

    MESH TERMS: chemistry

    Chemical & Substance for Abstract: De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Information

    Substance Name: Virginiamycin

    Registry Number: 11006-76-1

    Grant and Affiliation Information for De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates.

    AFFILIATION: Department of Chemistry, West Virginia University, Morgantown, West Virginia 26506, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: GM63150

    ACRONYM: GM

    MEDLINETA: Org Lett

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    De novo formal synthesis of --virginiamycin M2 via the asymmetric hydration of dienoates Related Publications

     

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