S. E. Esipov

564 total citations
39 papers, 414 citations indexed

About

S. E. Esipov is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, S. E. Esipov has authored 39 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 12 papers in Molecular Biology and 7 papers in Pharmacology. Recurrent topics in S. E. Esipov's work include Synthesis and Characterization of Heterocyclic Compounds (8 papers), Synthesis and Biological Evaluation (8 papers) and Analytical Chemistry and Chromatography (5 papers). S. E. Esipov is often cited by papers focused on Synthesis and Characterization of Heterocyclic Compounds (8 papers), Synthesis and Biological Evaluation (8 papers) and Analytical Chemistry and Chromatography (5 papers). S. E. Esipov collaborates with scholars based in Russia, United States and Germany. S. E. Esipov's co-authors include M. N. Kolosov, Yu. A. Berlin, M. M. Shemyakin, В. И. Шейченко, S. G. Batrakov, В. В. Смирнов, I. P. Beletskaya, M G Brazhnikova, В. В. Смирнов and Е А Киприанова and has published in prestigious journals such as FEBS Letters, Chemical Physics Letters and Phytochemistry.

In The Last Decade

S. E. Esipov

35 papers receiving 391 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. E. Esipov Russia	14	167	158	64	50	44	39	414
Mark A. Minton United States	15	335 2.0×	312 2.0×	26 0.4×	78 1.6×	37 0.8×	30	762
Wibo B. van Scheppingen Netherlands	8	131 0.8×	92 0.6×	51 0.8×	30 0.6×	43 1.0×	16	350
T. G. Bonner United Kingdom	10	225 1.3×	141 0.9×	34 0.5×	31 0.6×	41 0.9×	57	465
Dong-Ni Wang Denmark	13	151 0.9×	70 0.4×	17 0.3×	82 1.6×	59 1.3×	40	422
Nobuya Tokutake Japan	14	104 0.6×	316 2.0×	51 0.8×	16 0.3×	21 0.5×	23	446
Kent E. Göklen United States	12	172 1.0×	366 2.3×	30 0.5×	45 0.9×	118 2.7×	17	613
A. Kergomard France	13	190 1.1×	263 1.7×	67 1.0×	19 0.4×	30 0.7×	61	484
Wesley Cocker Ireland	11	203 1.2×	181 1.1×	31 0.5×	36 0.7×	22 0.5×	78	466
David H. Grayson Ireland	13	219 1.3×	104 0.7×	21 0.3×	32 0.6×	23 0.5×	50	430
Aimé Cambon France	14	311 1.9×	190 1.2×	23 0.4×	91 1.8×	17 0.4×	52	706

Countries citing papers authored by S. E. Esipov

Since Specialization

Citations

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

Fields of papers citing papers by S. E. Esipov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. E. Esipov. 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 S. E. Esipov. The network helps show where S. E. Esipov may publish in the future.

Co-authorship network of co-authors of S. E. Esipov

This figure shows the co-authorship network connecting the top 25 collaborators of S. E. Esipov. A scholar is included among the top collaborators of S. E. Esipov 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 S. E. Esipov. S. E. Esipov 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

Смирнов, В. В., et al.. (2006). Fluviols, bicyclic nitrogen-rich antibiotics produced by Pseudomonas fluorescens. FEMS Microbiology Letters. 153(2). 357–361. 41 indexed citations

Batrakov, S. G., et al.. (2004). Lipids of the zygomycete Absidia corymbifera F-965. Phytochemistry. 65(9). 1239–1246. 14 indexed citations

Pivovarova, T. A., T. F. Kondrat’eva, S. G. Batrakov, et al.. (2003). [Phenotypic features of Ferroplasma acidiphilum strains Yt and Y-2].. PubMed. 71(6). 809–18. 21 indexed citations

Batrakov, S. G., et al.. (2003). A novel lipopeptide, an inhibitor of bacterial adhesion, from the thermophilic and halotolerant subsurface Bacillus licheniformis strain 603. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1634(3). 107–115. 42 indexed citations

Batrakov, S. G., et al.. (2002). β-D-Glucopyranosyl caldarchaetidylglycerol is the main lipid of the acidophilic, mesophilic, ferrous iron-oxidising archaeon Ferroplasma acidiphilum. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1581(1-2). 29–35. 25 indexed citations

Batrakov, S. G., et al.. (2002). Unusual fatty acid composition of cerebrosides from the filamentous soil fungus Mortierella alpina. Chemistry and Physics of Lipids. 117(1-2). 45–51. 23 indexed citations

Овчинникова, Т. В., et al.. (2002). Mitochondrial H+-ATPase: Identification of Subunits of the F0 Subcomplex that Contact Membrane Lipids. Russian Journal of Bioorganic Chemistry. 28(5). 371–384. 1 indexed citations

Будыка, М. Ф., et al.. (2002). Is C2 cluster ingested by fullerene C60?. Chemical Physics Letters. 354(1-2). 93–99. 20 indexed citations

Смирнов, В. В., et al.. (2001). Cluster Grignard Reagents. Organometallics. 20(12). 2449–2450. 24 indexed citations

10.

Esipov, S. E., et al.. (2001). Application of sulfur as a matrix for laser desorption/ionization in the characterization of halogenated fullerenes. Rapid Communications in Mass Spectrometry. 16(2). 99–102. 28 indexed citations

11.

Скворцов, В. Г., et al.. (1998). Synthesis and experimental pharmacokinetics of 3-14C-reumycin. Pharmaceutical Chemistry Journal. 32(5). 234–236.

12.

Esipov, S. E., et al.. (1988). Protonation of pyrimidotriazinediones by1H and13C NMR spectroscopy. Chemistry of Heterocyclic Compounds. 24(11). 1271–1277.

13.

Preobrazhenskaya, M. N., et al.. (1988). N-alkylation of 4-chloro-5-cyano-1,2,3-triazole with orthoformic acid derivatives. Chemistry of Heterocyclic Compounds. 24(7). 756–759.

14.

Esipov, S. E., et al.. (1987). Novel method for the synthesis of pyrido[2,3-d]pyrimidine-2,4-diones from 5,7-dimethylpyrimido[4,5-e]-1,2,4-triazine-6,8-dione. Chemistry of Heterocyclic Compounds. 23(12). 1370–1370. 1 indexed citations

15.

Esipov, S. E., et al.. (1987). Different modes of alkaline hydrolysis of fervenulin and isofervenulin. Chemistry of Heterocyclic Compounds. 23(11). 1247–1251. 1 indexed citations

16.

Aleksandrov, Grigory G., et al.. (1986). Structure and some properties of tetrazole 5-methylpyrimido[4,5-e]-[1,2,4]triazine-6,8-dione and its azide in different phase states. Chemistry of Heterocyclic Compounds. 22(1). 95–100. 2 indexed citations

17.

Александров, Г.Г., et al.. (1984). Alkaloids ofHypecoum erectum, the structure of hyperectine. Chemistry of Natural Compounds. 20(5). 592–598. 6 indexed citations

18.

Esipov, S. E., et al.. (1973). THE STRUCTURE OF REUMYCIN. The Journal of Antibiotics. 26(9). 537–538. 12 indexed citations

19.

Berlin, Yu. A., S. E. Esipov, О. А. Киселева, & M. N. Kolosov. (1967). Olivomycin and related antibiotics. Chemistry of Natural Compounds. 3(5). 280–285. 2 indexed citations

20.

Berlin, Yu. A., S. E. Esipov, M. N. Kolosov, & M. M. Shemyakin. (1966). The structure of the olivomycin-chromomycin antibiotics. Tetrahedron Letters. 7(15). 1643–1647. 25 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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