М. В. Дмитриев

1.3k total citations
220 papers, 943 citations indexed

About

М. В. Дмитриев is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, М. В. Дмитриев has authored 220 papers receiving a total of 943 indexed citations (citations by other indexed papers that have themselves been cited), including 201 papers in Organic Chemistry, 25 papers in Molecular Biology and 18 papers in Pharmacology. Recurrent topics in М. В. Дмитриев's work include Chemical synthesis and pharmacological studies (101 papers), Synthesis and Characterization of Pyrroles (49 papers) and Synthesis and Reactions of Organic Compounds (43 papers). М. В. Дмитриев is often cited by papers focused on Chemical synthesis and pharmacological studies (101 papers), Synthesis and Characterization of Pyrroles (49 papers) and Synthesis and Reactions of Organic Compounds (43 papers). М. В. Дмитриев collaborates with scholars based in Russia, United States and France. М. В. Дмитриев's co-authors include А. Н. Масливец, P. S. Silaichev, В. Л. Гейн, Victoria V. Grishko, Andrei N. Yankin, И. А. Толмачева, Michael Rubin, Павел А. Слепухин, З. Г. Алиев and В. А. Глушков and has published in prestigious journals such as SHILAP Revista de lepidopterología, Tetrahedron and Molecules.

In The Last Decade

М. В. Дмитриев

194 papers receiving 915 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
М. В. Дмитриев Russia 13 785 151 72 42 30 220 943
Rohan D. Erande India 14 440 0.6× 111 0.7× 90 1.3× 26 0.6× 39 1.3× 32 581
Gangavaram V. M. Sharma India 14 616 0.8× 180 1.2× 52 0.7× 30 0.7× 26 0.9× 23 685
А. Н. Масливец Russia 14 1.4k 1.8× 108 0.7× 52 0.7× 20 0.5× 22 0.7× 331 1.5k
Petros G. Tsoungas Greece 15 489 0.6× 170 1.1× 41 0.6× 48 1.1× 29 1.0× 54 636
Ramakrishna G. Bhat India 17 653 0.8× 167 1.1× 21 0.3× 30 0.7× 18 0.6× 56 720
Rodolfo D. Bravo Argentina 16 593 0.8× 371 2.5× 59 0.8× 28 0.7× 18 0.6× 52 641
Antonio Guirado Spain 14 548 0.7× 126 0.8× 21 0.3× 34 0.8× 15 0.5× 70 673
Gary D. Allred United States 6 709 0.9× 117 0.8× 70 1.0× 39 0.9× 29 1.0× 7 767
Nicolai A. Aksenov Russia 18 1.2k 1.5× 308 2.0× 32 0.4× 48 1.1× 9 0.3× 189 1.2k
Ayman W. Erian Egypt 16 937 1.2× 118 0.8× 39 0.5× 21 0.5× 18 0.6× 54 1.0k

Countries citing papers authored by М. В. Дмитриев

Since Specialization
Citations

This map shows the geographic impact of М. В. Дмитриев'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 М. В. Дмитриев with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites М. В. Дмитриев more than expected).

Fields of papers citing papers by М. В. Дмитриев

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by М. В. Дмитриев. 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 М. В. Дмитриев. The network helps show where М. В. Дмитриев may publish in the future.

Co-authorship network of co-authors of М. В. Дмитриев

This figure shows the co-authorship network connecting the top 25 collaborators of М. В. Дмитриев. A scholar is included among the top collaborators of М. В. Дмитриев 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 М. В. Дмитриев. М. В. Дмитриев is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Дмитриев, М. В., et al.. (2025). Synthesis and Electrophilic Heterocyclization of 3-(Allylsulfanyl)-1,2,4-triazino[6,5-b]indole. Russian Journal of Organic Chemistry. 61(1). 41–48.
3.
Khramtsov, Pavel, et al.. (2025). Acylpyruvates and Their Heterocyclic Derivatives as Growth Regulators in Chlorella vulgaris. BioTech. 14(4). 90–90.
4.
Майзлиш, В. Е., et al.. (2024). 8-(4-(3,4-Dicyano)phenoxyphenyl)-2,6-diethyl-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene: Synthesis and photophysical properties. Optical Materials. 159. 116558–116558. 2 indexed citations
5.
Дмитриев, М. В., et al.. (2024). Nonlinearity of the heterogeneous process of zinc release in flow Batteries. SHILAP Revista de lepidopterología. 531. 1023–1023.
6.
Дмитриев, М. В., et al.. (2023). Stereoselective Epoxidation of Triterpenic Allylic Alcohols and Cytotoxicity Evaluation of Synthesized Compounds. Molecules. 28(2). 550–550. 3 indexed citations
7.
Дмитриев, М. В., et al.. (2023). Potassium Trifluorotris(pentafluoroethyl)phosphate. SHILAP Revista de lepidopterología. 2023(3). M1687–M1687.
8.
Дмитриев, М. В., et al.. (2023). Synthesis of 1-Antipyryl-1H-pyrrol-2-ones by Reaction of N-Antipyryl-Substituted Enamines with Oxalyl Chloride. Russian Journal of Organic Chemistry. 59(4). 647–651. 3 indexed citations
9.
Дмитриев, М. В., et al.. (2023). Nucleophile-induced ring contraction in pyrrolo[2,1-c][1,4]benzothiazines: access to pyrrolo[2,1-b][1,3]benzothiazoles. Beilstein Journal of Organic Chemistry. 19. 646–657. 2 indexed citations
10.
Дмитриев, М. В., et al.. (2023). Synthesis of 1-antipyryl-1<i>H</i>-pyrrol-2-ones by interaction <i>N</i>-antipyryl substituted enamines with oxalyl chloride. Журнал органической химии. 59(4). 535–540. 1 indexed citations
11.
Гейн, В. Л., et al.. (2023). Biginelli Reaction in the Synthesis of Ethyl 4-(6-Aryl-5-benzoyl-4-hydroxy-2-thioxohexahydropyrimidine-4-carboxamido)benzoates. Russian Journal of General Chemistry. 93(1). 16–21. 1 indexed citations
12.
Дмитриев, М. В., Alexander S. Novikov, Irina D. Yushina, et al.. (2023). Nonlinear Metal–Organic Framework Crystals for Efficient Multicolor Coherent Optical Emission. Advanced Optical Materials. 11(22). 19 indexed citations
13.
Гейн, В. Л., et al.. (2023). Synthesis of substituted cyclohexenones by reaction of chalcones with acetoacetic acid amides. Журнал Общей Химии. 93(11). 1664–1671.
14.
Дмитриев, М. В., et al.. (2021). NOVEL APPROACH TO THE SYNTHESIS OF 3-AMINO-4-ARYLPYRIDIN-2(1 H )-ONE DERIVATIVES. Chemistry of Heterocyclic Compounds. 57. 764–771. 1 indexed citations
15.
Yankin, Andrei N., et al.. (2021). Straightforward synthesis of novel spiroether derivatives. Synthetic Communications. 51(11). 1731–1741. 12 indexed citations
16.
Дмитриев, М. В., et al.. (2020). Synthesis of 1,4-benzothiazinones from acylpyruvic acids or furan-2,3-diones and o-aminothiophenol. Beilstein Journal of Organic Chemistry. 16. 2322–2331. 14 indexed citations
17.
Mashevskaya, I. V., et al.. (2020). Nucleophilic Addition of Oxindole toPyrroloquinoxalinetriones. Russian Journal of Organic Chemistry. 56(4). 719–722. 1 indexed citations
18.
Дмитриев, М. В., et al.. (2018). Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases. Beilstein Journal of Organic Chemistry. 14. 1734–1742. 6 indexed citations
19.
Дмитриев, М. В., et al.. (2018). Synthesis and Intramolecular Cyclization of a 2,3-seco-Oleanane Triterpenoid with an Ethylketone Fragment. Chemistry of Natural Compounds. 54(6). 1094–1099. 5 indexed citations
20.
Дмитриев, М. В., et al.. (2016). Structure of 3-methyl-2,3,4,4a,5, 10b-hexahydro-1H-spiro[chromeno[3,4-c] pyridin-1,1'-cyclohexane]-2,4,5-trione. Journal of Structural Chemistry. 57(6). 1263–1265. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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