Sergey S. Zhokhov

739 total citations
38 papers, 558 citations indexed

About

Sergey S. Zhokhov is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Sergey S. Zhokhov has authored 38 papers receiving a total of 558 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 11 papers in Molecular Biology and 7 papers in Physiology. Recurrent topics in Sergey S. Zhokhov's work include Cyclopropane Reaction Mechanisms (8 papers), Alzheimer's disease research and treatments (7 papers) and Asymmetric Synthesis and Catalysis (6 papers). Sergey S. Zhokhov is often cited by papers focused on Cyclopropane Reaction Mechanisms (8 papers), Alzheimer's disease research and treatments (7 papers) and Asymmetric Synthesis and Catalysis (6 papers). Sergey S. Zhokhov collaborates with scholars based in Russia, Tajikistan and United States. Sergey S. Zhokhov's co-authors include Alexander Makarov, Sergey A. Kozin, Vladimir I. Polshakov, Alexey B. Mantsyzov, Аlbert T. Lebedev, Alexandra A. Kulikova, Annalisa Pastore, Tatiana Yu. Samgina, Petr I. Matveev and Maria I. Indeykina and has published in prestigious journals such as Angewandte Chemie International Edition, Scientific Reports and Food Chemistry.

In The Last Decade

Sergey S. Zhokhov

37 papers receiving 548 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sergey S. Zhokhov Russia	12	205	177	90	78	71	38	558
Laurent Sabater France	12	198 1.0×	220 1.2×	94 1.0×	49 0.6×	106 1.5×	20	509
Paulina González United States	12	163 0.8×	191 1.1×	57 0.6×	83 1.1×	112 1.6×	16	527
Valeria Lanza Italy	15	236 1.2×	221 1.2×	38 0.4×	117 1.5×	94 1.3×	29	573
Jong‐Min Suh South Korea	11	82 0.4×	119 0.7×	58 0.6×	151 1.9×	51 0.7×	19	398
Alice Santoro France	8	108 0.5×	132 0.7×	47 0.5×	57 0.7×	152 2.1×	12	392
Amandine Conte‐Daban France	12	110 0.5×	256 1.4×	44 0.5×	43 0.6×	135 1.9×	12	449
Cheal Kim South Korea	11	243 1.2×	122 0.7×	42 0.5×	67 0.9×	27 0.4×	24	574
Quentin I. Churches Australia	13	246 1.2×	140 0.8×	25 0.3×	202 2.6×	76 1.1×	17	614
Michael R. Jones Canada	10	135 0.7×	179 1.0×	29 0.3×	129 1.7×	49 0.7×	14	461
Kornelia Wiśniewska Poland	10	254 1.2×	320 1.8×	46 0.5×	34 0.4×	154 2.2×	12	598

Countries citing papers authored by Sergey S. Zhokhov

Since Specialization

Citations

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

Fields of papers citing papers by Sergey S. Zhokhov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergey S. Zhokhov

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

1.

Zhokhov, Sergey S., В. А. Тафеенко, Иван А. Андреев, et al.. (2024). Converting Strain Release into Aromaticity Loss for Activation of Donor–Acceptor Cyclopropanes: Generation of Quinone Methide Traps for C-Nucleophiles. Organic Letters. 26(38). 8177–8182. 4 indexed citations

2.

Андреев, Иван А., Нина К. Ратманова, Sergey S. Zhokhov, et al.. (2024). Synthesis and evaluation of tetrahydropyrrolo[1,2- a ]quinolin-1(2 H )-ones as new tubulin polymerization inhibitors. RSC Medicinal Chemistry. 16(1). 274–285. 2 indexed citations

3.

Zhokhov, Sergey S., et al.. (2023). A simple method for the synthesis of isoindoline derivatives. Chemistry of Heterocyclic Compounds. 59(1-2). 54–62. 3 indexed citations

4.

Андреев, Иван А., et al.. (2023). Concise approach to γ-(het)aryl- and γ-alkenyl-γ-aminobutyric acids. Synthesis of vigabatrin. Organic & Biomolecular Chemistry. 22(5). 1027–1033. 2 indexed citations

5.

Zhokhov, Sergey S., Victor B. Rybakov, Иван А. Андреев, et al.. (2023). Donor–Acceptor Cyclopropane Ring Expansion to 1,2-Dihydronaphthalenes. Access to Bridged Seven-Membered Lactones. Organic Letters. 25(44). 7963–7967. 3 indexed citations

6.

Adzhubei, Alexei A., Maria I. Indeykina, Igor Popov, et al.. (2023). Molecular Mechanism of Zinc-Dependent Oligomerization of Alzheimer’s Amyloid-β with Taiwan (D7H) Mutation. International Journal of Molecular Sciences. 24(14). 11241–11241. 5 indexed citations

7.

Zhokhov, Sergey S., et al.. (2022). Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines. Molecules. 27(23). 8468–8468. 5 indexed citations

8.

Zhokhov, Sergey S., et al.. (2022). Ring expansion of donor—acceptor cyclopropanes bearing arylcarbamoyl group into 1,5-diarylpyrrolidin-2-ones. Russian Chemical Bulletin. 71(11). 2431–2440. 6 indexed citations

9.

Андреев, Иван А., Alexey O. Chagarovskiy, Ирина И. Левина, et al.. (2019). Ring Opening of Donor–Acceptor Cyclopropanes with Cyanide Ion and Its Surrogates. The Journal of Organic Chemistry. 85(2). 1146–1157. 29 indexed citations

10.

Kozin, Sergey A., Vladimir I. Polshakov, Yuri V. Mezentsev, et al.. (2018). Enalaprilat Inhibits Zinc-Dependent Oligomerization of Metal-Binding Domain of Amyloid-beta Isoforms and Protects Human Neuroblastoma Cells from Toxic Action of these Isoforms. Molecular Biology. 52(4). 590–597. 11 indexed citations

11.

Ustynyuk, N.A., Dmitry N. Zarubin, F.M. Dolgushin, et al.. (2018). New benzo[f]quinolino[3,4-b][1,7]naphthyridine-6,8(5H,9H)-diones: synthesis, electronic, molecular, and crystal structures. Protonation and complexation with lanthanum and europium salts. Russian Chemical Bulletin. 67(10). 1878–1890. 3 indexed citations

12.

Polshakov, Vladimir I., Alexey B. Mantsyzov, Sergey A. Kozin, et al.. (2017). A Binuclear Zinc Interaction Fold Discovered in the Homodimer of Alzheimer's Amyloid‐β Fragment with Taiwanese Mutation D7H. Angewandte Chemie International Edition. 56(39). 11734–11739. 26 indexed citations

13.

Polshakov, Vladimir I., Alexey B. Mantsyzov, Sergey A. Kozin, et al.. (2017). A Binuclear Zinc Interaction Fold Discovered in the Homodimer of Alzheimer's Amyloid‐β Fragment with Taiwanese Mutation D7H. Angewandte Chemie. 129(39). 11896–11901. 4 indexed citations

14.

Kozin, Sergey A., Sergey S. Zhokhov, Alexey B. Mantsyzov, et al.. (2016). Interplay of histidine residues of the Alzheimer’s disease Aβ peptide governs its Zn-induced oligomerization. Scientific Reports. 6(1). 21734–21734. 85 indexed citations

15.

Vinogradov, Eugeny V., Nikita G. Sedush, Tigran S. Kurtikyan, et al.. (2016). Intermolecular interactions in rifabutin–2-hydroxypropyl-β-cyclodextrin–water solutions, according to solubility data. Russian Journal of Physical Chemistry A. 90(5). 983–989. 1 indexed citations

16.

Kulikova, Alexandra A., Philipp O. Tsvetkov, Maria I. Indeykina, et al.. (2014). Phosphorylation of Ser8 promotes zinc-induced dimerization of the amyloid-β metal-binding domain. Molecular BioSystems. 10(10). 2590–2596. 46 indexed citations

17.

Сторожева, З. И., A. T. Proshin, Sergey S. Zhokhov, et al.. (2006). Hexapeptides HLDF-6 and PEDF-6 restore memory in rats after chronic intracerebroventricular treatment with β-amyloid peptide Aβ(25–35). Bulletin of Experimental Biology and Medicine. 141(3). 319–322. 6 indexed citations

18.

Zhokhov, Sergey S., I. A. Коstanyan, З. И. Сторожева, et al.. (2004). Different Mechanisms of Protective and Differentiative Activities of Homological Peptides TGENHR and TQVEHR. Biochemistry (Moscow). 69(8). 861–869. 7 indexed citations

19.

Zhokhov, Sergey S., et al.. (2004). HLDF-6 peptide affects behavioral reactions and organism functions dependent on androgen hormones in normal and castrated male mice. Regulatory Peptides. 127(1-3). 111–121. 11 indexed citations

20.

Zhokhov, Sergey S., et al.. (2000). [Biological role of a neurotrophic factor fragment from pigment epithelium: structure-functional homology with a differentiation factor for the HL-60 cell line].. PubMed. 26(8). 563–70.

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