Russian Journal of Organic Chemistry

Papers
(The H4-Index of Russian Journal of Organic Chemistry is 11. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-09-01 to 2025-09-01.)
ArticleCitations
Regioselective Synthesis of Furocoumarin Derivatives and Their Docking and ADME Studies for Alzheimer’s Disease32
DBU-Catalyzed Efficient One-Pot Three-Component Synthesis of Aminoquinoline Derivatives via Betti Reaction in Polar Medium and Antidiabetic Activity of the Products29
Synthesis of Functionally Substituted 4H-Thiopyrans by Reaction of Carbon Disulfide with Malononitrile Trimer27
Antiepileptic Drug Rufinamide: Synthesis and Process Impurities26
Straightforward Synthesis of 6-Aryl-2-azido-4-(trifluoromethyl)­pyrimidines and Their Regioselective Copper-Catalyzed Click Cycloaddition to 6-Aryl-2-(4-phenyl-1H-1,2,3-triazol-1-yl)-4-(trifluoromethy20
Silica-Zinc Chloride (SiO2-ZnCl2)-Mediated Facile Synthesis of Some Nitro-Substituted Arylimidazopyridine Analogs19
Synthesis and Molecular Docking Study of Arylsulfanyl Pyrazolylpyrazoline Derivatives as Antitubercular Agents17
One-Pot Three-Component Green Synthesis of (Z)-5-Benzylidene-3-methyl(phenyl)-2,5-dihydro-1,2,4-triazin-6(1H)-ones14
Synthesis, Crystal Structures, and Cytotoxic Activity of Two Acetyl Chroman Derivatives13
Synthesis, Identification, and Evaluation of New Pyrimidine and Pyrazole Derivatives Bearing a Quinazolin-4(3H)-one Moiety, Including Antibacterial, Antifungal, and Antioxidant Effects12
A Practical Transition Metal-Free Synthesis of Highly Substituted Thiophenes Containing a Benzoxazole Moiety and Their Antimicrobial Activity12
Synthesis of Pregnane–Cholesterol and Cholesterol–Cholesterol Prodrugs via Ring A–Ring A Connection. Potential Cytotoxic Activity against Cervical Cancer Cell Line HeLa11
Uncommon Ozonolysis of 2,3-Seco-24,28-dinorlupa-4(23),20(29)-diene-2,17-dicarbonitrile11
Efficient Multicomponent Synthesis of Methyl 2-(Benzyloxy)-5-[2-(2-{[3-(substituted phenyl)-1-phenyl-1H-pyrazol-4-yl]­methylidene}hydrazinyl)-1,3-thiazol-4-yl]benzoates11
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