An enantioselective approach to (-)-platencin via catalytic asymmetric intramolecular cyclopropanation

Sho Hirai, Masahisa Nakada

    Research output: Contribution to journal › Article

    39 Citations (Scopus)

    Abstract

    This Letter describes an enantioselective approach to (-)-platencin. A uniquely functionalized chiral intermediate, which was prepared via the highly enantioselective catalytic asymmetric intramolecular cyclopropanation (CAIMCP) that we have developed, was successfully transformed to Nicolaou's intermediate in his total synthesis of (-)-platencin.

    Original languageEnglish
    Pages (from-to)5076-5079
    Number of pages4
    JournalTetrahedron Letters
    Volume51
    Issue number38
    DOIs
    Publication statusPublished - 2010

    Fingerprint

    platencin

    ASJC Scopus subject areas

    • Biochemistry
    • Organic Chemistry
    • Drug Discovery

    Cite this

    An enantioselective approach to (-)-platencin via catalytic asymmetric intramolecular cyclopropanation. / Hirai, Sho; Nakada, Masahisa.

    In: Tetrahedron Letters, Vol. 51, No. 38, 2010, p. 5076-5079.

    Research output: Contribution to journal › Article

    Hirai, S & Nakada, M 2010, 'An enantioselective approach to (-)-platencin via catalytic asymmetric intramolecular cyclopropanation', Tetrahedron Letters, vol. 51, no. 38, pp. 5076-5079. https://doi.org/10.1016/j.tetlet.2010.07.088
    Hirai S, Nakada M. An enantioselective approach to (-)-platencin via catalytic asymmetric intramolecular cyclopropanation. Tetrahedron Letters. 2010;51(38):5076-5079. https://doi.org/10.1016/j.tetlet.2010.07.088
    Hirai, Sho ; Nakada, Masahisa. / An enantioselective approach to (-)-platencin via catalytic asymmetric intramolecular cyclopropanation. In: Tetrahedron Letters. 2010 ; Vol. 51, No. 38. pp. 5076-5079.
    @article{c2ed9fbf7a3c443980a8d1415faccff9,
    title = "An enantioselective approach to (-)-platencin via catalytic asymmetric intramolecular cyclopropanation",
    abstract = "This Letter describes an enantioselective approach to (-)-platencin. A uniquely functionalized chiral intermediate, which was prepared via the highly enantioselective catalytic asymmetric intramolecular cyclopropanation (CAIMCP) that we have developed, was successfully transformed to Nicolaou's intermediate in his total synthesis of (-)-platencin.",
    author = "Sho Hirai and Masahisa Nakada",
    year = "2010",
    doi = "10.1016/j.tetlet.2010.07.088",
    language = "English",
    volume = "51",
    pages = "5076--5079",
    journal = "Tetrahedron Letters",
    issn = "0040-4039",
    publisher = "Elsevier Limited",
    number = "38",

    }

    TY - JOUR

    T1 - An enantioselective approach to (-)-platencin via catalytic asymmetric intramolecular cyclopropanation

    AU - Hirai, Sho

    AU - Nakada, Masahisa

    PY - 2010

    Y1 - 2010

    N2 - This Letter describes an enantioselective approach to (-)-platencin. A uniquely functionalized chiral intermediate, which was prepared via the highly enantioselective catalytic asymmetric intramolecular cyclopropanation (CAIMCP) that we have developed, was successfully transformed to Nicolaou's intermediate in his total synthesis of (-)-platencin.

    AB - This Letter describes an enantioselective approach to (-)-platencin. A uniquely functionalized chiral intermediate, which was prepared via the highly enantioselective catalytic asymmetric intramolecular cyclopropanation (CAIMCP) that we have developed, was successfully transformed to Nicolaou's intermediate in his total synthesis of (-)-platencin.

    UR - http://www.scopus.com/inward/record.url?scp=78549272004&partnerID=8YFLogxK

    UR - http://www.scopus.com/inward/citedby.url?scp=78549272004&partnerID=8YFLogxK

    U2 - 10.1016/j.tetlet.2010.07.088

    DO - 10.1016/j.tetlet.2010.07.088

    M3 - Article

    AN - SCOPUS:78549272004

    VL - 51

    SP - 5076

    EP - 5079

    JO - Tetrahedron Letters

    JF - Tetrahedron Letters

    SN - 0040-4039

    IS - 38

    ER -

    Access to Document