Л. Н. Диваева

619 total citations
93 papers, 460 citations indexed

About

Л. Н. Диваева is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, Л. Н. Диваева has authored 93 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Organic Chemistry, 25 papers in Molecular Biology and 15 papers in Oncology. Recurrent topics in Л. Н. Диваева's work include Synthesis and Biological Evaluation (22 papers), Synthesis and Characterization of Heterocyclic Compounds (21 papers) and Synthesis and biological activity (17 papers). Л. Н. Диваева is often cited by papers focused on Synthesis and Biological Evaluation (22 papers), Synthesis and Characterization of Heterocyclic Compounds (21 papers) and Synthesis and biological activity (17 papers). Л. Н. Диваева collaborates with scholars based in Russia, Belarus and Greece. Л. Н. Диваева's co-authors include А. С. Морковник, А. С. Бурлов, Т. А. Кузьменко, Г. С. Бородкин, В. Г. Карцев, А. Д. Гарновский, А. И. Ураев, Igor S. Vasilchenko, Konstantin А. Lyssenko and Varvara V. Avdeeva and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Physical Chemistry B and International Journal of Molecular Sciences.

In The Last Decade

Л. Н. Диваева

86 papers receiving 452 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Л. Н. Диваева Russia	10	285	135	100	96	82	93	460
Abbas Pezeshk United States	12	115 0.4×	195 1.4×	121 1.2×	111 1.2×	89 1.1×	33	437
Uddhavesh B. Sonawane India	7	239 0.8×	375 2.8×	122 1.2×	161 1.7×	71 0.9×	7	500
MF Mackay Australia	11	231 0.8×	75 0.6×	78 0.8×	67 0.7×	37 0.5×	41	394
Cecı́lia P. Sár Hungary	12	131 0.5×	37 0.3×	32 0.3×	140 1.5×	34 0.4×	32	433
V.K. Landry United States	7	283 1.0×	80 0.6×	174 1.7×	17 0.2×	72 0.9×	7	381
L.M. Hryhorczuk United States	9	92 0.3×	176 1.3×	141 1.4×	58 0.6×	77 0.9×	14	346
SinChun Lim Australia	8	69 0.2×	172 1.3×	71 0.7×	108 1.1×	21 0.3×	9	526
Manjuri Kumar India	11	202 0.7×	217 1.6×	84 0.8×	93 1.0×	33 0.4×	16	349
Joanna Will Germany	8	250 0.9×	305 2.3×	45 0.5×	171 1.8×	18 0.2×	8	526
Shuji Masumoto Japan	13	626 2.2×	46 0.3×	246 2.5×	177 1.8×	12 0.1×	19	754

Countries citing papers authored by Л. Н. Диваева

Since Specialization

Citations

This map shows the geographic impact of Л. Н. Диваева's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Л. Н. Диваева with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Л. Н. Диваева more than expected).

Fields of papers citing papers by Л. Н. Диваева

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Л. Н. Диваева. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Л. Н. Диваева. The network helps show where Л. Н. Диваева may publish in the future.

Co-authorship network of co-authors of Л. Н. Диваева

This figure shows the co-authorship network connecting the top 25 collaborators of Л. Н. Диваева. A scholar is included among the top collaborators of Л. Н. Диваева based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Л. Н. Диваева. Л. Н. Диваева is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kubasov, Alexey S., Lyudmila V. Goeva, А. С. Бурлов, et al.. (2025). Benzimidazole-containing silver(I) complexes: Synthesis, structure, features of complexation. Inorganica Chimica Acta. 588. 122862–122862.

Mahalapbutr, Panupong, Athina Geronikaki, В. Г. Карцев, et al.. (2024). Discovery of furopyridine-based compounds as novel inhibitors of Janus kinase 2: In silico and in vitro studies. International Journal of Biological Macromolecules. 260. 129308–129308. 7 indexed citations

Карцев, В. Г., Panupong Mahalapbutr, Athina Geronikaki, et al.. (2024). Furopyridine Derivatives as Potent Inhibitors of the Wild Type, L858R/T790M, and L858R/T790M/C797S EGFR. The Journal of Physical Chemistry B. 128(50). 12389–12402. 3 indexed citations

Kubasov, Alexey S., А. С. Бурлов, Л. Н. Диваева, et al.. (2024). Silver(I) complexation with N-donor heterocyclic ligands in the presence of boron cluster anions: Synthesis and coordination features. Polyhedron. 263. 117209–117209. 1 indexed citations

Angeli, Andrea, Anthi Petrou, В. Г. Карцев, et al.. (2024). Phthalazine Sulfonamide Derivatives as Carbonic Anhydrase Inhibitors. Synthesis, Biological and in silico Evaluation. ChemMedChem. 19(15). e202400147–e202400147. 3 indexed citations

Диваева, Л. Н., et al.. (2023). β-Carbolines as intermediates in indirect heteroarylation of tryptamines exemplified by the synthesis of 2-pyrazolyltryptamines. Mendeleev Communications. 33(5). 645–647.

Kubasov, Alexey S., Yu. V. Koshchienko, А. С. Бурлов, et al.. (2023). Schiff Base Derivatives in Zinc(II) and Cadmium(II) Complexation with the closo-Dodecaborate Anion. Crystals. 13(10). 1449–1449. 1 indexed citations

Карцев, В. Г., Panupong Mahalapbutr, Anthi Petrou, et al.. (2023). Discovery of Novel EGFR Inhibitor Targeting Wild-Type and Mutant Forms of EGFR: In Silico and In Vitro Study. Molecules. 28(7). 3014–3014. 11 indexed citations

Kubasov, Alexey S., И. В. Козерожец, А. С. Бурлов, et al.. (2023). Luminescent cadmium(II) complexes with benzyl and chlorobenzyl benzimidazole derivatives and closo-decaborate anion. Inorganica Chimica Acta. 557. 121654–121654. 7 indexed citations

10.

Диваева, Л. Н., et al.. (2023). Диазепинобензимидазолы — новый класс для поиска соединений с акнсиолитической активностью. Экспериментальная и клиническая фармакология. 86(11s). 101a–101a.

11.

Морковник, А. С., et al.. (2023). New β-[o-(5-oxopyrazol-3-yl)aryl]ethylamines and their unusual metastable betaine form. Mendeleev Communications. 33(2). 203–205. 1 indexed citations

12.

Карцев, В. Г., Athina Geronikaki, Anthi Petrou, et al.. (2022). Synthesis and Antimicrobial Activity of New Heteroaryl(aryl) Thiazole Derivatives Molecular Docking Studies. Antibiotics. 11(10). 1337–1337. 19 indexed citations

13.

Карцев, В. Г., Anthi Petrou, Athina Geronikaki, et al.. (2022). Experimental and In Silico Evaluation of New Heteroaryl Benzothiazole Derivatives as Antimicrobial Agents. Antibiotics. 11(11). 1654–1654. 5 indexed citations

14.

Спасов, А. А., et al.. (2022). Design, Synthesis and Pharmacological Evaluation of Novel C2,C3-Quinoxaline Derivatives as Promising Anxiolytic Agents. International Journal of Molecular Sciences. 23(22). 14401–14401. 3 indexed citations

15.

Zhuravlev, Konstantin P., Vera I. Tsaryuk, Alexey S. Kubasov, et al.. (2021). Crystal structures, luminescence, and DFT study of mixed-ligand Zn(II) and Cd(II) complexes with phenyl-containing benzimidazole derivatives with linker C N or N N group. Journal of Luminescence. 237. 118156–118156. 29 indexed citations

16.

Спасов, А. А., et al.. (2021). Searching for new anxiolytic agents among derivatives of 11-dialkylaminoethyl-2,3,4,5-tetrahydrodiazepino[1,2-a]benzimidazole. European Journal of Pharmaceutical Sciences. 161. 105792–105792. 8 indexed citations

17.

Спасов, А. А., et al.. (2019). Antithrombotic Activity of a Novel Diazepino[1,2-α] Benzimidazole Derivative on Arterial Thrombosis Model in Rats without Concomitant Pathology and in Rats with Experimental Myocardial Infarction. Bulletin of Experimental Biology and Medicine. 166(6). 747–750. 1 indexed citations

18.

Спасов, А. А., et al.. (2017). Antithrombotic Activity of DAB-15, a Novel Diazepinobenzimidazole Compound. Bulletin of Experimental Biology and Medicine. 162(5). 636–639. 2 indexed citations

19.

Зарубаев, Владимир В., et al.. (2016). Tautomeric and non-tautomeric N-substituted 2-iminobenzimidazolines as new lead compounds for the design of anti-influenza drugs: An in vitro study. Bioorganic & Medicinal Chemistry. 24(22). 5796–5803. 6 indexed citations

20.

Ураев, А. И., A.L. Nivorozhkin, Л. Н. Диваева, et al.. (2003). Synthesis and structures of iron(iii) complexes based on azo derivatives of 5-oxo- and 5-thioxopyrazole. Russian Chemical Bulletin. 52(11). 2523–2526. 8 indexed citations

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