Current Organic Synthesis

Papers
(The H4-Index of Current Organic Synthesis is 16. 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 2022-08-01 to 2026-08-01.)
ArticleCitations
Ultrasound-assisted and Efficient Multicomponent Synthesis of 4H-Pyran Derivatives Catalyzed by LiOH.H2O in Water59
Omega Indices of Strong and Lexicographic Products of Graphs32
Beyond 1,2,3-triazoles: Formation and Applications of Ketemines Derived from Copper Catalyzed Azide Alkyne Cycloaddition31
Efficient Generation of Specific Counting Polynomials and their Subsequent Indices of Complex Boric Acid Structure27
A Review on Novel Synthesis Approaches and Biological Activities of 1,2,4- Oxadiazole and 1,3,4-Oxadiazole Tailored Compounds26
GOQDs and GOQDs-NS-doped Carbocatalysts: A Concise Study on Production and Use in One-pot Green MCRs26
Research Progress on the Application of Nanocellulose in Glucose Sensing25
Acknowledgements to Reviewers23
Synthesis, Anti-acetylcholinesterase Evaluation, Molecular Docking and Molecular Dynamics Simulation of Novel Psoralen Derivatives20
Synthesis and Characterization of 3-S-impurities in Timolol Maleate20
Efficient Formylation of Alcohols Using a Core-Shell Magnetic Nanocomposite Via Vilsmeier-Haack Complex Formation20
Concise Synthesis and Nematicidal Activity Evaluation of Waltherione S and its Derivatives against Meloidogyne incognita20
Synthesis of Isatin Derivatives Exhibiting Antibacterial, Antifungal and Cytotoxic Activities19
Development of a Scalable and High-yield Process for the Synthesis of Decitabine19
Antiphytopathogenic Effects and the Preliminary Mechanisms of 5-nitro-8-hydroxyquinoline Derivatives17
Synthesis, Reaction and Biological Activity of Thiazoles16
Design, Synthesis, QSAR Studies, and Molecular Modeling of Some Novel Bis Methyl 2-[3-(benzo[d]thiazol-2-yl)-2-terephthaloyl-bis-4-oxo-thiazolidin- 5-ylidene]acetates and Screening of their Antioxidan16
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