Yu. N. Bubnov

1.5k total citations
181 papers, 1.1k citations indexed

About

Yu. N. Bubnov is a scholar working on Organic Chemistry, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Yu. N. Bubnov has authored 181 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 152 papers in Organic Chemistry, 36 papers in Molecular Biology and 29 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Yu. N. Bubnov's work include Organoboron and organosilicon chemistry (55 papers), Chemical Synthesis and Reactions (30 papers) and Boron Compounds in Chemistry (29 papers). Yu. N. Bubnov is often cited by papers focused on Organoboron and organosilicon chemistry (55 papers), Chemical Synthesis and Reactions (30 papers) and Boron Compounds in Chemistry (29 papers). Yu. N. Bubnov collaborates with scholars based in Russia, Ukraine and Hungary. Yu. N. Bubnov's co-authors include M. E. Gurskii, B. M. Mikhaĭlov, S. V. Baranin, А. В. Игнатенко, Yan Z. Voloshin, Nikolai Yu. Kuznetsov, O. P. Novikova, A. A. Prishchenko, М. В. Ливанцов and L. I. Livantsova and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and Tetrahedron.

In The Last Decade

Yu. N. Bubnov

156 papers receiving 1.0k citations

Peers

Yu. N. Bubnov
Graham Taylor United Kingdom
Gregory B. Boursalian United States
David Whittaker United Kingdom
Ross S. Robinson South Africa
Yu. N. Bubnov
Citations per year, relative to Yu. N. Bubnov Yu. N. Bubnov (= 1×) peers Paola Del Buttero

Countries citing papers authored by Yu. N. Bubnov

Since Specialization
Citations

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

Fields of papers citing papers by Yu. N. Bubnov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yu. N. Bubnov

This figure shows the co-authorship network connecting the top 25 collaborators of Yu. N. Bubnov. A scholar is included among the top collaborators of Yu. N. Bubnov 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 Yu. N. Bubnov. Yu. N. Bubnov 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.
Bubnov, Yu. N., A. A. Prishchenko, М. В. Ливанцов, et al.. (2025). Oxirane-based synthesis of functionalized derivatives of 2-hydroxyalkyl-substituted organophosphorus acids. Russian Chemical Bulletin. 74(2). 489–502.
2.
Bubnov, Yu. N., A. A. Prishchenko, М. В. Ливанцов, et al.. (2025). Imine-based synthesis of functionalized phosphorus-containing carboxamides. Russian Chemical Bulletin. 74(1). 171–189.
3.
Bubnov, Yu. N., A. A. Prishchenko, М. В. Ливанцов, et al.. (2024). Synthesis of functionalized organophosphorus analogs of glycine containing PCH2N units. Russian Chemical Bulletin. 73(6). 1725–1737. 3 indexed citations
4.
Bubnov, Yu. N., A. A. Prishchenko, М. В. Ливанцов, et al.. (2024). Hexahydro-1,3,5-triazine-based synthesis of functionalized phosphorus-substituted dialkylamides of organophosphorus acids. Russian Chemical Bulletin. 73(12). 3647–3657.
5.
Bubnov, Yu. N., A. A. Prishchenko, М. В. Ливанцов, et al.. (2024). Synthesis of functionalized organophosphorus derivatives of succinic acid. Russian Chemical Bulletin. 73(8). 2339–2349. 2 indexed citations
6.
Bubnov, Yu. N., A. A. Prishchenko, М. В. Ливанцов, et al.. (2024). Enamine-based synthesis of functionalized aminoalkyl compounds bearing 3-, 4- or 5-coordinated phosphorus atom. Russian Chemical Bulletin. 73(7). 1953–1961. 3 indexed citations
7.
Bubnov, Yu. N., A. A. Prishchenko, М. В. Ливанцов, et al.. (2024). Synthesis of functionalized N-acylated amino acids containing 3- and 4-coordinated phosphorus moieties. Russian Chemical Bulletin. 73(10). 3012–3026.
8.
Prishchenko, A. A., М. В. Ливанцов, O. P. Novikova, et al.. (2023). Synthesis of ferrocene-containing phosphonous and phosphinic acids based on alkenylferrocenes. Russian Chemical Bulletin. 72(8). 1849–1854. 14 indexed citations
9.
Prishchenko, A. A., М. В. Ливанцов, O. P. Novikova, et al.. (2023). Synthesis of functionalized trimethylsilyl aminomethylphosphinates containing triethoxysilyl moieties. Russian Chemical Bulletin. 72(4). 1088–1092. 19 indexed citations
10.
Prishchenko, A. A., М. В. Ливанцов, O. P. Novikova, et al.. (2023). Synthesis of functionalized furan-containing phosphonous and phosphinic acids. Russian Chemical Bulletin. 72(9). 2138–2147. 14 indexed citations
11.
Komkov, A. V., et al.. (2019). Synthesis of new trichloromethyl- and alkoxy-substituted pyrido[2,3-d]pyrimidine derivatives. Russian Chemical Bulletin. 68(2). 365–373. 8 indexed citations
12.
Kuznetsov, Nikolai Yu. & Yu. N. Bubnov. (2014). Ruthenium-catalyzed intramolecular metathesis of dienes and its application in the synthesis of bridged and spiro azabicycles. Russian Chemical Reviews. 84(7). 758–785. 11 indexed citations
13.
Varzatskii, Оleg А., Valentin V. Novikov, Alexander S. Belov, et al.. (2014). Copper-promoted reductive homocoupling of quasi-aromatic iron(ii) clathrochelates: boosting the inhibitory activity in a transcription assay. Chemical Communications. 50(24). 3166–3166. 28 indexed citations
14.
Monakov, Yu. B., et al.. (2009). Ferrocenyl-containing iron(ii) clathrochelate-benzoyl peroxide, a new initiating system for radical polymerization of methyl methacrylate. Russian Chemical Bulletin. 58(6). 1162–1165. 1 indexed citations
15.
Voloshin, Yan Z., Ilya S. Makarov, Анна В. Вологжанина, et al.. (2008). Template synthesis and structures of bis-ferrocenylboronate macrobicyclic iron(ii) tris-dioximates. Russian Chemical Bulletin. 57(6). 1223–1230. 1 indexed citations
16.
Gurskii, M. E., et al.. (2005). The first preparation of (1S,5R)-(−)- and (1R,5S)-(+)-7-phenyl-3-borabicyclo[3.3.1]non-6-enes and their application for synthesis of chiral cyclohexene derivatives. Journal of Organometallic Chemistry. 690(11). 2840–2846. 4 indexed citations
17.
Kotelnikova, R. A., et al.. (2004). Enantiomers of the Amino Acid Derivatives of Fullerene C60 Possess Stereospecific Membranotropic Properties. Doklady Biochemistry and Biophysics. 396(1-6). 165–167. 4 indexed citations
18.
Gridnev, Ilya D., Oleg L. Tok, M. E. Gurskii, & Yu. N. Bubnov. (1996). First observation of a [1,7] boron shift - Three independent fluxional processes in the tricarbonyliron complex of cycloheptatrienyl(dipropyl)borane. Angewandte Chemie International Edition. 108(21). 1483–1488. 6 indexed citations
19.
Bubnov, Yu. N., et al.. (1985). Organoboron compounds. Journal of Organometallic Chemistry. 292(1-2). 93–104. 6 indexed citations
20.
Mikhaĭlov, B. M., et al.. (1967). Organoboron compounds. Russian Chemical Bulletin. 16(10). 2193–2199. 3 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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