A. N. Reznikov

628 total citations
54 papers, 347 citations indexed

About

A. N. Reznikov is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, A. N. Reznikov has authored 54 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Organic Chemistry, 18 papers in Inorganic Chemistry and 10 papers in Molecular Biology. Recurrent topics in A. N. Reznikov's work include Asymmetric Synthesis and Catalysis (17 papers), Asymmetric Hydrogenation and Catalysis (15 papers) and Organophosphorus compounds synthesis (10 papers). A. N. Reznikov is often cited by papers focused on Asymmetric Synthesis and Catalysis (17 papers), Asymmetric Hydrogenation and Catalysis (15 papers) and Organophosphorus compounds synthesis (10 papers). A. N. Reznikov collaborates with scholars based in Russia. A. N. Reznikov's co-authors include Yu. N. Klimochkin, Victor B. Rybakov, Vadim A. Shiryaev, М. В. Леонова, Nikolay I. Bormotov, Elena I. Ivleva, Dmitry V. Osipov, V. A. Osyanin, Shishkina Ln and Н. С. Зефиров and has published in prestigious journals such as Tetrahedron, Tetrahedron Letters and European Journal of Medicinal Chemistry.

In The Last Decade

A. N. Reznikov

44 papers receiving 335 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. N. Reznikov Russia 11 299 109 52 36 26 54 347
V. Jagadeshwar India 9 407 1.4× 53 0.5× 52 1.0× 15 0.4× 14 0.5× 12 428
Isabel Merino Spain 16 585 2.0× 99 0.9× 91 1.8× 11 0.3× 39 1.5× 31 660
Trevor L. Calkins United States 11 478 1.6× 130 1.2× 132 2.5× 43 1.2× 19 0.7× 14 525
Ryo Mizojiri Japan 13 384 1.3× 57 0.5× 76 1.5× 12 0.3× 10 0.4× 20 456
Sunaina Sharma Canada 13 375 1.3× 92 0.8× 85 1.6× 10 0.3× 22 0.8× 16 452
M. Pilar Ruiz Spain 14 488 1.6× 50 0.5× 75 1.4× 15 0.4× 19 0.7× 29 505
Sudharshan Madapa India 10 488 1.6× 42 0.4× 160 3.1× 21 0.6× 19 0.7× 18 571
Christopher J. Bungard United States 9 216 0.7× 53 0.5× 40 0.8× 13 0.4× 15 0.6× 13 253
Kyle D. Reichl United States 10 310 1.0× 153 1.4× 68 1.3× 8 0.2× 16 0.6× 13 370
François-René Alexandre France 11 457 1.5× 60 0.6× 233 4.5× 41 1.1× 19 0.7× 17 585

Countries citing papers authored by A. N. Reznikov

Since Specialization
Citations

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

Fields of papers citing papers by A. N. Reznikov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. N. Reznikov. 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 A. N. Reznikov. The network helps show where A. N. Reznikov may publish in the future.

Co-authorship network of co-authors of A. N. Reznikov

This figure shows the co-authorship network connecting the top 25 collaborators of A. N. Reznikov. A scholar is included among the top collaborators of A. N. Reznikov 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 A. N. Reznikov. A. N. Reznikov 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.
Shiryaev, Vadim A., et al.. (2025). Asymmetric Synthesis of Isoindolin-1-ones from Enamides via Pd-Catalyzed Intramolecular Reductive Heck Reaction. Russian Journal of General Chemistry. 95(1). 30–34.
2.
Reznikov, A. N., et al.. (2024). Palladium-catalyzed cyclization of N-(2-iodophenyl)acrylamides and hydrophosphoryl compounds in the presence of (R,R)-DIOP and (S)-Monophos ligands. Russian Chemical Bulletin. 73(9). 2701–2707. 2 indexed citations
3.
Reznikov, A. N., et al.. (2023). Synthesis of 1-(Adamantan-1-yl)propane-1,2-diamine and Chiral Ligands Based Thereon. Russian Journal of Organic Chemistry. 59(3). 383–394.
4.
Shiryaev, Vadim A., et al.. (2021). Synthesis of non-racemic dihydrofurans via Ni(II)-catalyzed asymmetric Michael addition. Tetrahedron. 84. 132029–132029. 13 indexed citations
6.
Reznikov, A. N., et al.. (2018). Nitroalkenes in the Ni(II) Catalyzed AsymmetricMichaelAddition. Convenient Route to the Key Intermediate of Brivaracetam. Helvetica Chimica Acta. 101(12). 12 indexed citations
7.
Shiryaev, Vadim A., Eugene V. Radchenko, Vladimir A. Palyulin, et al.. (2018). Molecular design, synthesis and biological evaluation of cage compound-based inhibitors of hepatitis C virus p7 ion channels. European Journal of Medicinal Chemistry. 158. 214–235. 36 indexed citations
8.
Shiryaev, Vadim A., et al.. (2018). Asymmetric Synthesis of Adamantyl GABA Analogues. Synthesis. 51(2). 463–469. 7 indexed citations
9.
Reznikov, A. N., et al.. (2017). Enantioselective addition of β-keto phosphinate to ω-nitrostyrene in the presence of optically active nickel(II) complex. Russian Journal of Organic Chemistry. 53(2). 153–156. 6 indexed citations
10.
Reznikov, A. N., et al.. (2016). Synthesis of Ni(II) complexes with chiral derivatives of cyclohexane-1,2-diamine, bycyclo[2.2.2]octane-2,3-diamine, and 1,2-diphenylethane-1,2-diamine. Russian Journal of General Chemistry. 86(11). 2477–2483. 1 indexed citations
11.
Reznikov, A. N., et al.. (2013). Enantioselective synthesis of γ-aminobutyric acid derivatives by Ni(II)-catalyzed reaction of diethyl malonate with nitroalkenes. Russian Journal of Organic Chemistry. 49(5). 663–668. 21 indexed citations
12.
Reznikov, A. N., et al.. (2012). Enantioselective addition of diethyl malonate to ω-nitrostyrenes in the presence of cobalt and manganese complexes with N,N′-dibenzyl-(1S,2S)-cyclohexane-1,2-diamine. Russian Journal of General Chemistry. 82(11). 1827–1829. 6 indexed citations
13.
Reznikov, A. N., et al.. (2010). Hydrosilylation of 3,3,4,4-tetrafluorohexa-1,5-diene and 4-bromo-3,3,4,4-tetrafluorobut-1-ene. Russian Journal of General Chemistry. 80(6). 1210–1212. 1 indexed citations
14.
Reznikov, A. N., et al.. (2010). Synthesis of 1-adamantyloxyalkanols. Russian Journal of Organic Chemistry. 46(11). 1741–1742. 5 indexed citations
15.
Klimochkin, Yu. N., et al.. (2009). Nucleoside Phosphonate Analogues Modified by Lipophilic Cage Moiety as Potential Antiviral Agents. Antiviral Research. 82(2). A60–A60. 1 indexed citations
16.
17.
Reznikov, A. N., et al.. (2008). Synthesis of 5-[3-(diphenylphosphinoyl)propyl]-2-thiobarbituric acid. Russian Journal of General Chemistry. 78(2). 320–322. 2 indexed citations
18.
Reznikov, A. N., et al.. (2007). Catalytic hydrophosphorylation of dialkyl 2-allylmalonates. Russian Journal of General Chemistry. 77(7). 1170–1176. 5 indexed citations
19.
Reznikov, A. N., et al.. (1966). Temperature in a wedge due to a source of variable size and strength. Journal of Engineering Physics. 10(6). 419–421.
20.
Reznikov, A. N., et al.. (1965). Distribution of heat flux intensity and temperature on contact surfaces of moving bodies (as applied to cutting of metals). Journal of Engineering Physics and Thermophysics. 9(5). 363–366. 1 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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