The first total synthesis and structural determination of lagunamycin

Seijiro Hosokawa, Shoichi Kuroda, Keisuke Imamura, Kuniaki Tatsuta

    研究成果: Article

    25 引用 (Scopus)

    抄録

    Lagunamycin (1) has been synthesized by using our developed remote stereoinduction, Knorr condensation, periodinane oxidation, and diazonation. This enantioselective synthesis determined the absolute configuration of lagunamycin. Existence of rotational conformers was confirmed by NMR studies.

    元の言語English
    ページ(範囲)6183-6186
    ページ数4
    ジャーナルTetrahedron Letters
    47
    発行部数35
    DOI
    出版物ステータスPublished - 2006 8 28

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    Condensation
    Nuclear magnetic resonance
    Oxidation
    lagunamycin

    ASJC Scopus subject areas

    • Biochemistry
    • Organic Chemistry
    • Drug Discovery

    これを引用

    The first total synthesis and structural determination of lagunamycin. / Hosokawa, Seijiro; Kuroda, Shoichi; Imamura, Keisuke; Tatsuta, Kuniaki.

    :: Tetrahedron Letters, 巻 47, 番号 35, 28.08.2006, p. 6183-6186.

    研究成果: Article

    Hosokawa, Seijiro ; Kuroda, Shoichi ; Imamura, Keisuke ; Tatsuta, Kuniaki. / The first total synthesis and structural determination of lagunamycin. :: Tetrahedron Letters. 2006 ; 巻 47, 番号 35. pp. 6183-6186.
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