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10 ta ish

Ish: Action of Nitrating Mixtures and Mineral Acids on the Quinoline Alkaloids Haplophyllidine and Anhydroperforine

  1. A short history of<i>SHELX</i>

    George M. Sheldrick

    MaqolaOchiq kirish2007215 iqtibos
    ABI

  2. Crystal structure refinement with<i>SHELXL</i>

    George M. Sheldrick

    MaqolaOchiq kirish2014189 iqtibos
    ABI

  3. Tables of bond lengths determined by X-ray and neutron diffraction. Part 1. Bond lengths in organic compounds

    Frank H. Allen, Olga Kennard, David G. Watson +3

    Maqola198778 iqtibos
    ABI

  4. Natural Compounds

    Shakhnoza S. Azimova, Marat S. Yunusov

    KitobPharmacological Effects of Medicinal Plants201210 iqtibos
    ABI

  5. Intramolecular Cyclization During Bromination of the Quinoline Alkaloid Haplophyllidine

    A. U. Ubaidullaev, Валентина И. Виноградова, Sherzod Zhurakulov +4

    MaqolaOchiq kirishAlkaloids: synthesis and pharmacologyChemistry of Natural Compounds20225 iqtibos
    ABI

  6. Synthesis of Derivatives of the 2-Arylquinoline Alkaloid Dubamine and their Cytotoxicity

    A. R. NIYAZMETOV, E. O. Terent’eva, U. B. Khamidova +3

    MaqolaCancer therapeutics and mechanismsChemistry of Natural Compounds20204 iqtibos
    ABI

  7. Quinoline-based antimalarial hybrid compounds

    Stéphanie Vandekerckhove, Matthias D’hooghe

    Sharh maqola20144 iqtibos
    ABI

  8. Quinoline as a Privileged Scaffold in Cancer Drug Discovery

    V. Raja Solomon, H. Lee

    Sharh maqola20113 iqtibos
    ABI

  9. The technology of the isolation of the alkaloids dubinidine and haplophylidine

    L. T. Avazmukhamedov, T. T. Shakirov, V. A. Tel'nov

    MaqolaOchiq kirish19662 iqtibos
    ABI

  10. Structure of perforine and haplophyllidine

    Z. Sh. Faizutdinova, I. A. Bessonova, S. Yu. Yunusov

    MaqolaOchiq kirish19671 iqtibos
    ABI