Yuri Shafran

503 total citations
24 papers, 361 citations indexed

About

Yuri Shafran is a scholar working on Organic Chemistry, Clinical Psychology and Toxicology. According to data from OpenAlex, Yuri Shafran has authored 24 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 11 papers in Clinical Psychology and 11 papers in Toxicology. Recurrent topics in Yuri Shafran's work include Forensic Toxicology and Drug Analysis (11 papers), Psychedelics and Drug Studies (11 papers) and Click Chemistry and Applications (7 papers). Yuri Shafran is often cited by papers focused on Forensic Toxicology and Drug Analysis (11 papers), Psychedelics and Drug Studies (11 papers) and Click Chemistry and Applications (7 papers). Yuri Shafran collaborates with scholars based in Russia, Bulgaria and Austria. Yuri Shafran's co-authors include Вадим А. Шевырин, Oleg S. Eltsov, Yu. Yu. Morzherin, Vasiliy А. Bakulev, Аlbert T. Lebedev, Павел А. Слепухин, Tetyana Beryozkina, Enrico Benassi, Gregory W. Endres and V. A. Bakulev and has published in prestigious journals such as Tetrahedron, Tetrahedron Letters and Analytical and Bioanalytical Chemistry.

In The Last Decade

Yuri Shafran

24 papers receiving 351 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuri Shafran Russia 11 211 158 113 110 65 24 361
Paul J. Dobrowolski United States 11 272 1.3× 242 1.5× 111 1.0× 79 0.7× 108 1.7× 18 473
Andrei Kornilov United States 9 129 0.6× 160 1.0× 119 1.1× 32 0.3× 60 0.9× 14 363
P. Anantha Reddy United States 10 145 0.7× 81 0.5× 93 0.8× 69 0.6× 165 2.5× 21 421
Carolina Noble Denmark 9 233 1.1× 120 0.8× 20 0.2× 82 0.7× 73 1.1× 12 335
Karolina Sekuła Poland 10 296 1.4× 84 0.5× 20 0.2× 201 1.8× 76 1.2× 14 376
Karin Tietje United States 13 87 0.4× 161 1.0× 172 1.5× 31 0.3× 187 2.9× 16 450
Donna M. Iula United States 8 111 0.5× 53 0.3× 46 0.4× 25 0.2× 75 1.2× 15 280
Lysbeth H. Antonides United Kingdom 10 257 1.2× 166 1.1× 6 0.1× 69 0.6× 85 1.3× 12 356
John D. Power Ireland 15 404 1.9× 70 0.4× 22 0.2× 219 2.0× 155 2.4× 31 555
Anders Just Pedersen Denmark 10 237 1.1× 83 0.5× 6 0.1× 112 1.0× 101 1.6× 13 390

Countries citing papers authored by Yuri Shafran

Since Specialization
Citations

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

Fields of papers citing papers by Yuri Shafran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yuri Shafran. 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 Yuri Shafran. The network helps show where Yuri Shafran may publish in the future.

Co-authorship network of co-authors of Yuri Shafran

This figure shows the co-authorship network connecting the top 25 collaborators of Yuri Shafran. A scholar is included among the top collaborators of Yuri Shafran 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 Yuri Shafran. Yuri Shafran 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.
Шевырин, Вадим А., et al.. (2024). Identification of thermolabile positional isomers of N‐(2‐hydroxybenzyl)‐2‐(dimethoxyphenyl)ethanamines (NBOH series) using chromatography and mass spectrometry methods. Drug Testing and Analysis. 16(11). 1271–1284. 1 indexed citations
2.
Bakulev, Vasiliy А., et al.. (2022). Heterocyclic azides: advances in their chemistry. Russian Chemical Reviews. 91(7). RCR5042–RCR5042. 10 indexed citations
3.
Shafran, Yuri, Aqeel A. Hussein, Вадим А. Шевырин, et al.. (2022). Selective Synthesis of Azoloyl NH-1,2,3-Triazoles and Azolyl Diazoketones: Experimental and Computational Insights. ACS Omega. 7(6). 5008–5031. 4 indexed citations
5.
Shafran, Yuri, P. S. Silaichev, & V. A. Bakulev. (2019). β-(Cycloalkylamino)ethanesulfonyl azides as novel water-soluble reagents for the synthesis of diazo compounds and heterocycles. Chemistry of Heterocyclic Compounds. 55(12). 1251–1261. 7 indexed citations
6.
Bakulev, Vasiliy А., Yuri Shafran, & Wim Dehaen. (2019). Progress in intermolecular and intramolecular reactions of thioamides with diazo compounds and azides. Tetrahedron Letters. 60(7). 513–523. 17 indexed citations
7.
Shafran, Yuri, et al.. (2019). Synthesis of β-azolyl- and β-azolylcarbonylenamines and their reactions with aromatic azides. Chemistry of Heterocyclic Compounds. 55(8). 704–715. 7 indexed citations
8.
Medvedev, Jury J., et al.. (2017). Rh(II)-mediated domino [4 + 1]-annulation of α-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes. Beilstein Journal of Organic Chemistry. 13. 2569–2576. 7 indexed citations
9.
Шевырин, Вадим А. & Yuri Shafran. (2017). Distinguishing of 2‐MAPB and 6‐MAPB: Solution of the problem. Journal of Mass Spectrometry. 52(10). 633–637. 4 indexed citations
11.
Shafran, Yuri, et al.. (2016). Synthesis of Assemblies of Isoxazole and Azoles Based on 1,3-Dipolar Cycloaddition Reaction of Enamines with Nitrile Oxides. Chemistry of Heterocyclic Compounds. 52(9). 743–749. 6 indexed citations
12.
Шевырин, Вадим А., et al.. (2015). Identification and analytical characteristics of synthetic cannabinoids with an indazole-3-carboxamide structure bearing a N-1-methoxycarbonylalkyl group. Analytical and Bioanalytical Chemistry. 407(21). 6301–6315. 50 indexed citations
13.
Шевырин, Вадим А., et al.. (2015). Synthetic cannabinoid 3-benzyl-5-[1-(2-pyrrolidin-1-ylethyl)-1H-indol-3-yl]-1,2,4-oxadiazole. The first detection in illicit market of new psychoactive substances. Forensic Science International. 259. 95–100. 18 indexed citations
14.
Beryozkina, Tetyana, Yuri Shafran, Gert Lübec, et al.. (2015). A novel transformation of β-1,2,3-thiadiazol-5-yl enamines into thieno[2,3-d]pyridazines. Tetrahedron Letters. 56(12). 1545–1547. 5 indexed citations
16.
Beryozkina, Tetyana, Yuri Shafran, Oleg S. Eltsov, et al.. (2014). Self-condensation of β-(isoxazol-5-yl) enamines under treatment with acetyl chloride and acids. Synthesis of novel 1,3-diisoxazolyl-1,3-dieneamines and 1,3,5-triisoxazolyl benzenes. Tetrahedron. 70(25). 3915–3923. 6 indexed citations
18.
Шевырин, Вадим А., et al.. (2013). Analytical characterization of some synthetic cannabinoids, derivatives of indole-3-carboxylic acid. Forensic Science International. 232(1-3). 1–10. 42 indexed citations
19.
Шевырин, Вадим А., et al.. (2012). Identification and analytical properties of new synthetic cannabimimetics bearing 2,2,3,3-tetramethylcyclopropanecarbonyl moiety. Forensic Science International. 226(1-3). 62–73. 34 indexed citations
20.
Shafran, Yuri, Tetyana Beryozkina, Oleg S. Eltsov, et al.. (2012). Self condensation of enamines mediated by acetylation. A novel approach to 1-(azol-5-yl)-(1E,3Z)-butadiene-4-N,N-dimethylamines. Organic & Biomolecular Chemistry. 10(30). 5795–5795. 8 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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