The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes

Kazumasa Kanda, Tamami Koike, Kohei Endo, Takanori Shibata

    研究成果: Article

    32 引用 (Scopus)

    抄録

    The double Sonogashira coupling of diiodoparacyclophanes with alkynes proceeded to give planarly chiral dialkynylparacyclophanes; a chiral Pd catalyst, which was prepared in situ from PdCl2(CH 3CN)2 and Taniaphos, realized the first asymmetric Sonogashira coupling with up to ca. 80% ee.

    元の言語English
    ページ（範囲）1870-1872
    ページ数3
    ジャーナルChemical Communications
    発行部数14
    DOI
    出版物ステータスPublished - 2009

    Fingerprint

    Alkynes
    Chirality
    Catalysts
    palladium chloride

    ASJC Scopus subject areas

    • Metals and Alloys
    • Materials Chemistry
    • Surfaces, Coatings and Films
    • Electronic, Optical and Magnetic Materials
    • Ceramics and Composites
    • Catalysis
    • Chemistry(all)

    これを引用

    The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes. / Kanda, Kazumasa; Koike, Tamami; Endo, Kohei; Shibata, Takanori.

    ：: Chemical Communications, 番号 14, 2009, p. 1870-1872.

    研究成果: Article

    Kanda, K, Koike, T, Endo, K & Shibata, T 2009, 'The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes', Chemical Communications, 番号 14, pp. 1870-1872. https://doi.org/10.1039/b818904h
    Kanda K, Koike T, Endo K, Shibata T. The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes. Chemical Communications. 2009;(14):1870-1872. https://doi.org/10.1039/b818904h
    Kanda, Kazumasa ; Koike, Tamami ; Endo, Kohei ; Shibata, Takanori. / The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes. ：: Chemical Communications. 2009 ; 番号 14. pp. 1870-1872.
    @article{ce7d764877f0417ea8f7cd40d1033cbe,
    title = "The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes",
    abstract = "The double Sonogashira coupling of diiodoparacyclophanes with alkynes proceeded to give planarly chiral dialkynylparacyclophanes; a chiral Pd catalyst, which was prepared in situ from PdCl2(CH 3CN)2 and Taniaphos, realized the first asymmetric Sonogashira coupling with up to ca. 80{\%} ee.",
    author = "Kazumasa Kanda and Tamami Koike and Kohei Endo and Takanori Shibata",
    year = "2009",
    doi = "10.1039/b818904h",
    language = "English",
    pages = "1870--1872",
    journal = "Chemical Communications",
    issn = "1359-7345",
    publisher = "Royal Society of Chemistry",
    number = "14",

    }

    TY - JOUR

    T1 - The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes

    AU - Kanda, Kazumasa

    AU - Koike, Tamami

    AU - Endo, Kohei

    AU - Shibata, Takanori

    PY - 2009

    Y1 - 2009

    N2 - The double Sonogashira coupling of diiodoparacyclophanes with alkynes proceeded to give planarly chiral dialkynylparacyclophanes; a chiral Pd catalyst, which was prepared in situ from PdCl2(CH 3CN)2 and Taniaphos, realized the first asymmetric Sonogashira coupling with up to ca. 80% ee.

    AB - The double Sonogashira coupling of diiodoparacyclophanes with alkynes proceeded to give planarly chiral dialkynylparacyclophanes; a chiral Pd catalyst, which was prepared in situ from PdCl2(CH 3CN)2 and Taniaphos, realized the first asymmetric Sonogashira coupling with up to ca. 80% ee.

    UR - http://www.scopus.com/inward/record.url?scp=65249128332&partnerID=8YFLogxK

    UR - http://www.scopus.com/inward/citedby.url?scp=65249128332&partnerID=8YFLogxK

    U2 - 10.1039/b818904h

    DO - 10.1039/b818904h

    M3 - Article

    C2 - 19319429

    AN - SCOPUS:65249128332

    SP - 1870

    EP - 1872

    JO - Chemical Communications

    JF - Chemical Communications

    SN - 1359-7345

    IS - 14

    ER -

    文献にアクセス