E. A. Krasnokutskaya

951 total citations
38 papers, 603 citations indexed

About

E. A. Krasnokutskaya is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, E. A. Krasnokutskaya has authored 38 papers receiving a total of 603 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Organic Chemistry, 11 papers in Inorganic Chemistry and 7 papers in Molecular Biology. Recurrent topics in E. A. Krasnokutskaya's work include Synthesis and Biological Evaluation (17 papers), Chemical Synthesis and Reactions (12 papers) and Vanadium and Halogenation Chemistry (10 papers). E. A. Krasnokutskaya is often cited by papers focused on Synthesis and Biological Evaluation (17 papers), Chemical Synthesis and Reactions (12 papers) and Vanadium and Halogenation Chemistry (10 papers). E. A. Krasnokutskaya collaborates with scholars based in Russia, South Korea and Kazakhstan. E. A. Krasnokutskaya's co-authors include В. Д. Филимонов, Ki‐Whan Chi, Paul Knochel, Marina E. Trusova, Павел С. Постников, Hyunuk Kim, Young Min Lee, О. Х. Полещук, Ksenia S. Stankevich and Viktor V. Zhdankin and has published in prestigious journals such as Organic Letters, Tetrahedron Letters and Synthesis.

In The Last Decade

E. A. Krasnokutskaya

34 papers receiving 587 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. A. Krasnokutskaya Russia 13 480 115 101 63 61 38 603
Terrence J. Connolly Canada 13 373 0.8× 61 0.5× 91 0.9× 92 1.5× 116 1.9× 29 547
Pradeep S. Iyer United States 10 341 0.7× 125 1.1× 80 0.8× 50 0.8× 101 1.7× 17 518
Travis Remarchuk United States 9 352 0.7× 116 1.0× 112 1.1× 47 0.7× 40 0.7× 11 470
Serkan Eymür Türkiye 15 426 0.9× 113 1.0× 146 1.4× 52 0.8× 113 1.9× 51 677
Vincent Paul India 13 358 0.7× 196 1.7× 111 1.1× 22 0.3× 159 2.6× 18 605
Jason R. Schmink United States 15 498 1.0× 103 0.9× 103 1.0× 104 1.7× 77 1.3× 20 629
Rico Thorwirth Germany 6 395 0.8× 42 0.4× 136 1.3× 43 0.7× 94 1.5× 8 499
Anima Bose India 9 392 0.8× 78 0.7× 110 1.1× 42 0.7× 66 1.1× 11 517
Randall E. Robinson United States 11 288 0.6× 43 0.4× 76 0.8× 47 0.7× 101 1.7× 14 399
Błażej Dziuk Poland 14 335 0.7× 100 0.9× 59 0.6× 18 0.3× 114 1.9× 68 507

Countries citing papers authored by E. A. Krasnokutskaya

Since Specialization
Citations

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

Fields of papers citing papers by E. A. Krasnokutskaya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. A. Krasnokutskaya

This figure shows the co-authorship network connecting the top 25 collaborators of E. A. Krasnokutskaya. A scholar is included among the top collaborators of E. A. Krasnokutskaya 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 E. A. Krasnokutskaya. E. A. Krasnokutskaya 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.
2.
Krasnokutskaya, E. A., et al.. (2025). Synthesis, Structure, and Chemical Properties of 1-Oxidopyridinediazonium Sulfonates. Russian Journal of Organic Chemistry. 61(1). 60–72.
3.
Филимонов, В. Д., et al.. (2022). A Novel and Simple Synthesis of Ethers of Hydroxypyridines with Hexafluoropropan-2-ol via Diazotization of Aminopyridines and Aminoquinolines Under Acid-Free Conditions. Chemistry of Heterocyclic Compounds. 58(12). 721–726. 1 indexed citations
4.
Krasnokutskaya, E. A., et al.. (2020). A Novel One-Pot Synthesis of N,N-Dimethylaminopyridines by Diazotization of Aminopyridines in Dimethylformamide in the Presence of Trifluoromethanesulfonic Acid. Russian Journal of Organic Chemistry. 56(6). 1023–1028. 6 indexed citations
5.
6.
Krasnokutskaya, E. A., et al.. (2016). A new transformation of aminopyridines upon diazotization in acetonitrile with the formation of N-pyridinylacetamides. Russian Chemical Bulletin. 65(9). 2312–2314. 4 indexed citations
7.
Krasnokutskaya, E. A., et al.. (2015). N-chelate ruthenium carbene complexes in olefin metathesis and isomerization. Russian Journal of Organic Chemistry. 51(7). 907–909. 5 indexed citations
8.
Krasnokutskaya, E. A., et al.. (2015). A new type of ruthenium carbene complexes with N-chelating ligand. Russian Chemical Bulletin. 64(1). 44–47. 1 indexed citations
9.
10.
Krasnokutskaya, E. A., et al.. (2014). A new synthesis of pyridinyl trifluoromethanesulfonates via one-pot diazotization of aminopyridines in the presence of trifluoromethanesulfonic acid. Tetrahedron Letters. 55(28). 3771–3773. 12 indexed citations
11.
Филимонов, В. Д., О. Х. Полещук, E. A. Krasnokutskaya, & Gernot Frenking. (2011). DFT investigation of the thermodynamics and mechanism of electrophilic chlorination and iodination of arenes. Journal of Molecular Modeling. 17(11). 2759–2771. 17 indexed citations
12.
Chi, Ki‐Whan, et al.. (2011). A Green Procedure for the Diazotization-Iodination of Aromatic Amines under Aqueous, Strong-Acid-Free Conditions. Synthesis. 2011(13). 2154–2158. 11 indexed citations
13.
Филимонов, В. Д., et al.. (2008). Sulfonic Acid Based Cation-Exchange Resin: A Novel Proton Source for One-Pot Diazotization-Iodination of Aromatic Amines in Water. Synthesis. 2008(2). 185–187. 32 indexed citations
14.
Yusubov, Mekhman S., et al.. (2007). Solvent‐Free Iodination of Arenes Using Iodine—Silver Nitrate Combination.. ChemInform. 38(40).
15.
Филимонов, В. Д., et al.. (2007). Iodination of aryl amines in a water-paste form via stable aryl diazonium tosylates. Tetrahedron Letters. 49(6). 1080–1082. 43 indexed citations
16.
Krasnokutskaya, E. A., et al.. (2006). A New, One-Step, Effective Protocol for the Iodination of Aromatic and Heterocyclic Compounds via Aprotic Diazotization of Amines. Synthesis. 2007(1). 81–84. 112 indexed citations
17.
Филимонов, В. Д., et al.. (2006). Electronic structures and reactivities of iodinating agents in the gas phase and in solutions: A density functional study. Russian Chemical Bulletin. 55(8). 1328–1336. 15 indexed citations
18.
Krasnokutskaya, E. A., et al.. (2002). Convenient One‐Pot Oxidation of Acenaphthene into Acenaphthenequinone Using N‐Bromosuccinimide and DMSO.. ChemInform. 33(46). 129–129. 1 indexed citations
19.
Krasnokutskaya, E. A., et al.. (1995). アルケン類およびアルキン類を1,2‐ジケトン類へ酸化するDMSO系試薬. Bulletin of the Korean Chemical Society. 16(2). 86–88. 15 indexed citations
20.
Yusubov, Mekhman S., et al.. (1992). Oxidation, bromination, and methylenation of carbazole and (E)-3-(2-phenylethenyl)carbazole with HBr/DMSO. Chemistry of Heterocyclic Compounds. 28(11). 1260–1263. 2 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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