М. В. Проскурнина

442 total citations
40 papers, 353 citations indexed

About

М. В. Проскурнина is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, М. В. Проскурнина has authored 40 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Organic Chemistry, 9 papers in Molecular Biology and 6 papers in Pharmaceutical Science. Recurrent topics in М. В. Проскурнина's work include Fluorine in Organic Chemistry (6 papers), Inorganic and Organometallic Chemistry (4 papers) and Synthesis and Catalytic Reactions (4 papers). М. В. Проскурнина is often cited by papers focused on Fluorine in Organic Chemistry (6 papers), Inorganic and Organometallic Chemistry (4 papers) and Synthesis and Catalytic Reactions (4 papers). М. В. Проскурнина collaborates with scholars based in Russia, Tajikistan and France. М. В. Проскурнина's co-authors include N. S. Zefirov, Natalia A. Lozinskaya, Н. С. Зефиров, E. D. Matveeva, Sergey E. Tkachenko, I. F. LUTSENKO, Л. В. Аникина, Denis A. Babkov, T. D. Nekipelova and Andrew D. Mesecar and has published in prestigious journals such as Tetrahedron, Bioorganic & Medicinal Chemistry and Synthesis.

In The Last Decade

М. В. Проскурнина

37 papers receiving 345 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. Проскурнина Russia 10 224 83 72 64 24 40 353
Emanuele Rossini Germany 8 107 0.5× 108 1.3× 44 0.6× 53 0.8× 16 0.7× 8 310
Yao-Jung Chen Taiwan 12 571 2.5× 90 1.1× 45 0.6× 56 0.9× 22 0.9× 17 644
Américo Lemos Portugal 17 609 2.7× 50 0.6× 45 0.6× 117 1.8× 14 0.6× 36 676
Mark A. Olsen United States 10 289 1.3× 111 1.3× 52 0.7× 19 0.3× 32 1.3× 20 436
Wilford L. Mendelson United States 11 268 1.2× 108 1.3× 53 0.7× 38 0.6× 13 0.5× 26 354
Scott Savage United States 12 327 1.5× 140 1.7× 74 1.0× 40 0.6× 28 1.2× 21 446
Nemai C. Ganguly India 14 395 1.8× 113 1.4× 94 1.3× 33 0.5× 8 0.3× 38 470
David Tilly France 16 557 2.5× 107 1.3× 93 1.3× 35 0.5× 21 0.9× 27 667
Lissa T.J. Nelson United States 11 365 1.6× 142 1.7× 72 1.0× 54 0.8× 31 1.3× 12 531
Zehong Wan United States 12 311 1.4× 138 1.7× 102 1.4× 43 0.7× 31 1.3× 19 539

Countries citing papers authored by М. В. Проскурнина

Since Specialization
Citations

This map shows the geographic impact of М. В. Проскурнина'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. Проскурнина 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. Проскурнина more than expected).

Fields of papers citing papers by М. В. Проскурнина

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of М. В. Проскурнина. A scholar is included among the top collaborators of М. В. Проскурнина 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. Проскурнина. М. В. Проскурнина 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.
Lozinskaya, Natalia A., et al.. (2020). Synthesis and biotesting of new carrier prodrugs of 2-methoxyestradiol. Mendeleev Communications. 30(1). 7–9. 3 indexed citations
2.
Lozinskaya, Natalia A., Denis A. Babkov, Л. В. Аникина, et al.. (2019). Synthesis and biological evaluation of 3-substituted 2-oxindole derivatives as new glycogen synthase kinase 3β inhibitors. Bioorganic & Medicinal Chemistry. 27(9). 1804–1817. 33 indexed citations
3.
Аникина, Л. В., et al.. (2019). 2,4,5-Tris(alkoxyaryl)imidazoline derivatives as potent scaffold for novel p53-MDM2 interaction inhibitors: Design, synthesis, and biological evaluation. Bioorganic & Medicinal Chemistry Letters. 29(16). 2364–2368. 17 indexed citations
4.
Kuz’min, V. A., T. D. Nekipelova, М. В. Проскурнина, et al.. (2016). New phosphonate-substituted tricarbocyanines and their interaction with bovine serum albumin. Doklady Chemistry. 470(1). 264–267. 3 indexed citations
5.
Kuz’min, V. A., et al.. (2016). Synthesis of advanced fluorescent probes — water-soluble symmetrical tricarbocyanines with phosphonate groups. Russian Chemical Bulletin. 65(11). 2722–2728. 5 indexed citations
6.
7.
Kuz’min, V. A., Nikita A. Durandin, T. D. Nekipelova, et al.. (2015). Spectral and kinetic characteristics of indotricarbocyanine complexation with albumin. Doklady Physical Chemistry. 462(1). 107–109. 5 indexed citations
8.
Проскурнина, М. В., et al.. (2015). Homocoupling of bromotriazole derivatives on metal complex catalysts. Russian Chemical Bulletin. 64(6). 1470–1472. 3 indexed citations
9.
Kuz’min, V. A., Nikita A. Durandin, T. D. Nekipelova, et al.. (2015). Energy degradation in photoexcited complexes of indocarbocyanine with albumin. High Energy Chemistry. 49(3). 211–212. 7 indexed citations
10.
Lozinskaya, Natalia A., et al.. (2012). Synthesis of novel МТ3 receptor ligands via an unusual Knoevenagel condensation. Bioorganic & Medicinal Chemistry Letters. 22(24). 7578–7581. 22 indexed citations
11.
Lozinskaya, Natalia A., et al.. (2012). Stable synthetic equivalents of N-unsubstituted imines: Part 1. Synthesis. 2(1). 74–104. 2 indexed citations
12.
Lozinskaya, Natalia A., et al.. (2011). 1-Arylideneamino-2,2,2-trichloroethanols as synthetic equivalents of arylideneimines in the reaction with cyclopropenone derivatives. Russian Chemical Bulletin. 60(10). 1989–1994. 3 indexed citations
13.
Lozinskaya, Natalia A., et al.. (2010). Simple Synthesis of Some 2-Substituted Melatonin Derivatives. Synthesis. 2011(2). 273–276. 16 indexed citations
14.
Lozinskaya, Natalia A., et al.. (2009). Reaction of synthetic equivalents of arylideneimines, viz., 1-aryl- N,N’-bis(arylidene)methanediamines, with 2,3-diphenylcyclopropenone. Russian Chemical Bulletin. 58(1). 152–155. 6 indexed citations
15.
Тафеенко, В. А., et al.. (2009). 3-exo-Chloro-8-oxabicyclo[3.2.1]oct-6-ene-2,4-diol chloroform 0.33-solvate. Acta Crystallographica Section E Structure Reports Online. 65(7). o1580–o1580. 1 indexed citations
16.
Gleiter, Rolf, et al.. (2007). Insights into the Molecular Structure and Reactivity of α,ω‐Dialkoxy‐Substituted Ethyne and Butadiyne. European Journal of Organic Chemistry. 2007(35). 5834–5839. 10 indexed citations
17.
Matveeva, E. D., М. В. Проскурнина, & Н. С. Зефиров. (2006). Polyvalent iodine in organic chemistry: Recent developments, 2002–2005. Heteroatom Chemistry. 17(6). 595–617. 33 indexed citations
18.
Mironov, O. A., et al.. (2001). Reaction of Nitrogen(I) Oxide with Nitrogen-fixing Systems on the Basis of Lithium, Chlorotrimethylsilane, and Transition Metal Compounds. Russian Journal of General Chemistry. 71(6). 905–906. 1 indexed citations
19.
Khaikin, L. S., et al.. (1987). GAS-PHASE ELECTRON-DIFFRACTION STUDY OF 2-CHLORO-4,5-DIMETHYLL-1.3.2-DIOXAPHOSPHOLENE. Proceedings of the USSR Academy of Sciences. 296(1). 169–174. 3 indexed citations
20.
LUTSENKO, I. F. & М. В. Проскурнина. (1978). Organic Phosphorus Compounds with a P–P Bond. Russian Chemical Reviews. 47(9). 880–895. 13 indexed citations

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