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14 та иш

Иш: 1,2,4-Thiadiazol derivatives of cytisine alkaloid: solvate formation and phase transitions

  1. Phase annealing in SHELX-90: direct methods for larger structures

    George M. Sheldrick

    Мақола199045 иқтибос
    ABI

  2. Cytisine derivatives as ligands for neuronal nicotine receptors and with various pharmacological activities

    Caterina Canu Boido, Bruno Tasso, Vito Boido +1

    Шарҳ мақола200310 иқтибос
    ABI

  3. Structures of (−)-cytisine and (−)-N-methylcytisine: tricyclic quinolizidine alkaloids

    Andrew A. Freer, D. J. ROBINS, Gary N. Sheldrake

    Мақола198710 иқтибос
    ABI

  4. Relations between structure and nicotine‐like activity: X‐ray crystal structure analysis of (−)−cytisine and (−)−lobeline hydrochloride and a comparison with (−)−nicotine and other nicotine‐like compounds

    R. B. BARLOW, O. W. Johnson

    Мақола19899 иқтибос
    ABI

  5. Solution and crystal structure of cytisine, a quinolizidine alkaloid

    Paolo Mascagni, Marika Christodoulou, William A. Gibbons +4

    Мақола19878 иқтибос
    ABI

  6. Chemical Modification of Plant Alkaloids. III. X-Ray Diffraction and NMR Studies of the Structure of 1,3-Dimethyl-5-arylmethyl-5-cytisylmethylbarbituric Acids

    К. А. Краснов, В. Г. Карцев, A. S. Gorovoi +1

    Мақола20026 иқтибос
    ABI

  7. A proposal for the classification and nomenclature of host-guest-type compounds

    Edwin Weber, Hans‐Peter Josel

    Мақола19836 иқтибос
    ABI

  8. Crystal solvates and polymorphs of N-(3-methylthio-1,2,4-thiadiazol-5-yl-aminocarbonylmethyl)cytisine

    B. Tashkhodjave, K. K. Turgunov, Akmaljon Tojiboev +4

    МақолаNicotinic Acetylcholine Receptors StudyJournal of Inclusion Phenomena and Macrocyclic Chemistry20084 иқтибос
    ABI

  9. 1,2,4-Thiadiazole derivatives of cytisine

    V.A. Saprykina, Валентина И. Виноградова, R. F. Ambartsumova +3

    МақолаNicotinic Acetylcholine Receptors StudyChemistry of Natural Compounds20044 иқтибос
    ABI

  10. Anabasine and cytisine derivatives as reversible cholinesterase inhibitors

    A. G. Dobren'kov, Z. Tilyabaev, D. N. Dalimov +1

    Мақола19883 иқтибос
    ABI

  11. Optimization of parameters for semiempirical methods V: Modification of NDDO approximations and application to 70 elements

    James J. P. Stewart

    Мақола20073 иқтибос
    ABI

  12. Optimization of parameters for semiempirical methods I. Method

    James J. P. Stewart

    Мақола19892 иқтибос
    ABI

  13. Crystalsolvates of N-(3-ethylthio-1,2,4-thiadiazol-5-yl-aminocarbonylmethyl)cytisine

    U.S. Makhmudov, K. K. Turgunov, Б. Ташходжаев +2

    МақолаSynthesis and Reactivity of HeterocyclesChemistry of Natural Compounds20081 иқтибос
    ABI

  14. A new polymorphic form and crystal solvates of N-(3-methylthio-1,2,4-thiadiazol-5-yl-aminocarbonylmethyl)cytisine

    U.S. Makhmudov, K. K. Turgunov, B. Tashkhodjaev +3

    МақолаSynthesis and Reactivity of HeterocyclesJournal of Inclusion Phenomena and Macrocyclic Chemistry20091 иқтибос
    ABI