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Chemical Reaction Mechanisms

44 ta ish

  1. Time-dependent interaction of benzohydrazide with trifluoroacetyl-2-furanoylmethane: Hydrazone versus pyrazoline formation

    Elizaveta V. Panova, М. А. Турсунов, Maftuna J. Ruzieva +2

    MaqolaSynthesis and Characterization of PyrrolesJournal of Molecular Structure20265 iqtibos
    ABI

  2. Benzazoles. 3*. Synthesis and arylsulfonylation of 2-substituted benzimidazoles

    К. Б. Абдиреймов, Н. С. Мухамедов, М. Ж. Айымбетов +1

    MaqolaPhenothiazines and Benzothiazines Synthesis and ActivitiesChemistry of Heterocyclic Compounds20104 iqtibos
    ABI

  3. Quantum chemical studies of pyrimidin-4-ones 3. 2-Oxo(thioxo, selenoxo)pyrimidin-4-ones and 5,6-dimethyl-2-oxo(thioxo)thieno[2,3-d]pyrimidin-4-ones

    Mukhamatdin Mamarakhmonov, Л. И. Беленький, Н. Д. Чувылкин +2

    MaqolaSynthesis and Reactions of Organic CompoundsRussian Chemical Bulletin20143 iqtibos
    ABI

  4. Charge density of the biologically active molecule (2-oxo-1,3-benzoxazol-3(2<i>H</i>)-yl)acetic acid

    Ai Wang, Jamshid Ashurov, Aziz B. Ibragimov +4

    MaqolaSynthesis and Reactions of Organic CompoundsActa Crystallographica Section B Structural Science Crystal Engineering and Materials20162 iqtibos
    ABI

  5. Reductive dimerization of pyridine N-oxide

    A. S. Kurbatova, Yu. V. Kurbatov

    MaqolaChemical Synthesis and AnalysisChemistry of Heterocyclic Compounds19881 iqtibos
    ABI

  6. Reactions of 1,3-dihydrobenzo[c]thiophene 2,2-dioxides with electrophilic agents

    G.A. Tashbaev

    MaqolaOrganic Chemistry Cycloaddition ReactionsRussian Chemical Bulletin20051 iqtibos
    ABI

  7. Benzazoles 5*. Synthesis and arylsulfonylation of 1-hydroxymethylbenzimidazole

    К. Б. Абдиреймов, Н. С. Мухамедов, М. Ж. Айымбетов +1

    MaqolaSynthesis and biological activityChemistry of Heterocyclic Compounds20121 iqtibos
    ABI

  8. Benzazoles. 6*. Synthesis and Arylsulfonation of 2-Hydroxymethylbenzimidazole

    К. Б. Абдиреймов, Н. С. Мухамедов, R. Ya. Okmanov +3

    MaqolaChemical Reaction MechanismsChemistry of Heterocyclic Compounds20131 iqtibos
    ABI

  9. Molecular structure, HOMO-LUMO, MEP - – Analysis of triazine compounds using DFT (B3LYP) calculations

    Bakhtiyor Ganiev, Uktam Mardonov, Gulyayra Kholikova

    MaqolaSynthesis and Characterization of Heterocyclic CompoundsMaterials Today Proceedings20231 iqtibos
    ABI

  10. Addition of tetrahydrofuran to unsaturated acids

    G. G. Galust'yan, Ch. Sh. Kadyrov

    MaqolaChemical Reaction MechanismsChemistry of Heterocyclic Compounds19710 iqtibos
    ABI

  11. ChemInform Abstract: CHEMISTRY OF HETEROCYCLIC N‐OXIDES AND RELATED COMPOUNDS. 10. REACTION OF PYRIDINE N‐OXIDE WITH 4‐METHYL‐ AND 4‐PHENYL‐SUBSTITUTED HANTZSCH ESTERS

    A. S. Kurbatova, Yu. V. Kurbatov

    MaqolaChemical Reaction MechanismsChemischer Informationsdienst19790 iqtibos
    ABI

  12. Alkylation of a chiral hydrazone by means of asymmetric addition of Grignard reagents to the carbon-nitrogen double bond.

    Hiroshi Takahashi, Yuji Suzuki

    MaqolaOchiq kirishAnalytical Chemistry and ChromatographyChemical and Pharmaceutical Bulletin19830 iqtibos
    ABI

  13. Anticholinesterase properties of o-(?-alkoxyalkyl)-s-(n-butyl) methylthiophosphonates, O-(?-alkoxyalkyl)-S-(?-ethylthioethyl) methylthiophosphonates and their methyl sulfomethylates

    A. A. Abduvakhabov, O. Kh. Kholbekov, А. А. Садыков +2

    MaqolaOrganophosphorus compounds synthesisRussian Chemical Bulletin19830 iqtibos
    ABI

  14. ChemInform Abstract: Reaction of Substituted o‐Nitroanilines with Unsaturated Chlorine‐Containing Acids.

    L. V. Molchanov, A. T. Ayupova, Zh. Eshimbetov +1

    MaqolaChemical Reaction MechanismsChemInform19870 iqtibos
    ABI

  15. ChemInform Abstract: Reductive Dimerization of Pyridine N‐Oxide.

    A. S. Kurbatova, Yu. V. Kurbatov

    MaqolaChemical Reaction MechanismsChemInform19880 iqtibos
    ABI

  16. Protonation of triethyl (2-pyridylimido)phosphates

    R. U. Amanov, E. I. Matrosov, Mikhail Yu. Antipin +6

    MaqolaSynthesis and Reactivity of HeterocyclesRussian Chemical Bulletin19930 iqtibos
    ABI

  17. ChemInform Abstract: Novel Alkoxylation Reaction of Quinoline N‐Oxide.

    Yu. V. Kurbatov, S. N. KASYMOVA, R. A. TURAEVA

    MaqolaSynthesis and Biological EvaluationChemInform19930 iqtibos
    ABI

  18. ChemInform Abstract: Diphenylhydroxymethylation of 4‐Methylpyridine N‐Oxide with Benzophenone Ketylene and Dianions of Benzhydrol.

    D. A. Turaeva, A. S. Kurbatova, Yu. V. Kurbatov

    MaqolaOrganic Chemistry Cycloaddition ReactionsChemInform19940 iqtibos
    ABI

  19. ChemInform Abstract: New Reaction of Reductive Amination of Quinoline N‐Oxide with 2‐ Aminopyridine.

    M. A. Solekhova, Yu. V. Kurbatov

    MaqolaSynthesis and Biological EvaluationChemInform19970 iqtibos
    ABI

  20. ChemInform Abstract: Homolytic Addition of 1‐Alkanethiols to 5‐Ethynyl‐2‐methylpyridine.

    E. A. Il'yasov, G. G. Galust'yan

    MaqolaChemical Synthesis and ReactionsChemInform20000 iqtibos
    ABI

  21. ChemInform Abstract: Azabenzene Chemistry. Part 2. Methylation of 2,3‐Dihydrooxazolo[4,5‐b]pyridin‐2‐thione.

    Н. А. Алиев, М. Г. Левкович, Э. Л. Кристаллович +2

    MaqolaPhenothiazines and Benzothiazines Synthesis and ActivitiesChemInform20000 iqtibos
    ABI

  22. ChemInform Abstract: Nitration of Benzo Crown Ethers with Potassium Nitrate in Polyphosphoric Acid.

    A. D. Grebenyuk, Stanislav Andreev, I. A. Stempnevskaya +2

    MaqolaChemical Synthesis and ReactionsChemInform20010 iqtibos
    ABI

  23. Reductive Amination of Quinoline N‐Oxide with Aminopyridines and Their N‐Tosyl Derivatives.

    M. A. Solekhova, Yu. V. Kurbatov

    MaqolaSynthesis and Biological EvaluationChemInform20030 iqtibos
    ABI

  24. Synthesis of 5,6‐Diamino‐1,3‐dihydrobenzo[c]thiophene 2,2‐Dioxide.

    G.A. Tashbaev, O. Tukhtasunov

    MaqolaChemical Reaction MechanismsChemInform20060 iqtibos
    ABI

  25. Reaction of 1,3‐Dihydrobenzo[c]thiophene 2,2‐Dioxides with Electrophilic Agents.

    G.A. Tashbaev

    MaqolaOrganic Chemistry Cycloaddition ReactionsChemInform20060 iqtibos
    ABI