Ф. А. Валеев

607 total citations
96 papers, 483 citations indexed

About

Ф. А. Валеев is a scholar working on Organic Chemistry, Pharmacology and Oncology. According to data from OpenAlex, Ф. А. Валеев has authored 96 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Organic Chemistry, 21 papers in Pharmacology and 20 papers in Oncology. Recurrent topics in Ф. А. Валеев's work include Carbohydrate Chemistry and Synthesis (41 papers), Synthetic Organic Chemistry Methods (27 papers) and Cancer Treatment and Pharmacology (20 papers). Ф. А. Валеев is often cited by papers focused on Carbohydrate Chemistry and Synthesis (41 papers), Synthetic Organic Chemistry Methods (27 papers) and Cancer Treatment and Pharmacology (20 papers). Ф. А. Валеев collaborates with scholars based in Russia. Ф. А. Валеев's co-authors include М. С. Мифтахов, Irina N. Gaisina, Л. В. Спирихин, И. П. Цыпышева, Г. А. Толстиков, Anna Davidová, Е. В. Васильева, Ф. З. Галин, Д. В. Петров and В. А. Докичев and has published in prestigious journals such as Russian Chemical Reviews, Russian Chemical Bulletin and Mendeleev Communications.

In The Last Decade

Ф. А. Валеев

83 papers receiving 480 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ф. А. Валеев Russia 11 382 168 98 61 55 96 483
William S. Kissel United States 10 444 1.2× 210 1.3× 62 0.6× 40 0.7× 41 0.7× 13 580
Luke Humphreys United Kingdom 14 384 1.0× 365 2.2× 79 0.8× 48 0.8× 26 0.5× 31 658
Peter W. Sutton United Kingdom 13 199 0.5× 271 1.6× 40 0.4× 41 0.7× 48 0.9× 23 397
Monica Paravidino Netherlands 12 273 0.7× 278 1.7× 50 0.5× 32 0.5× 26 0.5× 17 454
P. Thirupathi Reddy India 10 369 1.0× 312 1.9× 60 0.6× 50 0.8× 19 0.3× 14 549
Thomas P. Tully United States 11 227 0.6× 330 2.0× 51 0.5× 29 0.5× 17 0.3× 15 480
Cynthia L. Rand United States 10 431 1.1× 235 1.4× 36 0.4× 33 0.5× 68 1.2× 12 618
V. A. Barkhash Russia 10 259 0.7× 126 0.8× 25 0.3× 57 0.9× 31 0.6× 75 416
Barbara Grischek Austria 16 331 0.9× 561 3.3× 125 1.3× 52 0.9× 33 0.6× 19 720
Sivappa Rasapalli United States 19 792 2.1× 231 1.4× 26 0.3× 97 1.6× 174 3.2× 49 925

Countries citing papers authored by Ф. А. Валеев

Since Specialization
Citations

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

Fields of papers citing papers by Ф. А. Валеев

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ф. А. Валеев. 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 Ф. А. Валеев. The network helps show where Ф. А. Валеев may publish in the future.

Co-authorship network of co-authors of Ф. А. Валеев

This figure shows the co-authorship network connecting the top 25 collaborators of Ф. А. Валеев. A scholar is included among the top collaborators of Ф. А. Валеев 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 Ф. А. Валеев. Ф. А. Валеев 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.
Валеев, Ф. А., et al.. (2025). Diels-Alder adduct of levoglucosenone and isoprene in the syntheses of the key synthon for loganin. Mendeleev Communications. 35(1). 57–59.
2.
Валеев, Ф. А., et al.. (2023). Reactions of cyrene with formaldehyde. Mendeleev Communications. 33(5). 648–649. 2 indexed citations
3.
Валеев, Ф. А., et al.. (2023). Regiocontrolled cleavage of the isocembrol cycle at the Δ2 bond and its transformation into 15-membered macrolide. Russian Chemical Bulletin. 72(10). 2466–2472. 1 indexed citations
4.
Валеев, Ф. А., et al.. (2023). Reactions of phenol and its derivatives with levoglucosenone. Chemistry of Heterocyclic Compounds. 59(4-5). 254–259. 1 indexed citations
5.
Валеев, Ф. А., et al.. (2023). Ene reaction of Diels–Alder adducts of levoglucosenone and 1,3-dienes with acetaldehyde. Mendeleev Communications. 33(1). 9–10. 1 indexed citations
6.
7.
Валеев, Ф. А., et al.. (2022). Synthesis of 4-Isopropyl Derivatives of Levoglucosenone. Russian Journal of Organic Chemistry. 58(12). 1797–1800.
8.
Валеев, Ф. А., et al.. (2022). Synthesis of 3,9-Dialkyl-1,8-cineole Derivatives Based on Diels–Alder Adducts of Levoglucosenone with Isoprene and Butadiene. Russian Journal of Organic Chemistry. 58(3). 295–305.
9.
Валеев, Ф. А., et al.. (2021). Synthesis of Purpurosamine TBDMS Ether from Cyrene™. Russian Journal of Organic Chemistry. 57(10). 1628–1631. 1 indexed citations
10.
Валеев, Ф. А., et al.. (2018). Michael Adduct of Levoglucosenone and Cyclohexanone. Chiral Protection of Hydroxy Group in Stereoselective Transformations of Glycol Aldehyde. Russian Journal of Organic Chemistry. 54(5). 726–733. 4 indexed citations
11.
Валеев, Ф. А., et al.. (2016). Eleuthesides and their analogs: XI. Final stage of the synthesis of sarcodictyin A analog with 14-methylcyclohex-12-ene ring A. Russian Journal of Organic Chemistry. 52(5). 721–726. 5 indexed citations
12.
Валеев, Ф. А., et al.. (2015). Synthesis of chiral 2,3-cis-fused butan-4-olides from levoglucosenone–1,3-diene Diels–Alder adducts. Mendeleev Communications. 25(4). 271–272. 10 indexed citations
13.
Спирихин, Л. В., et al.. (2014). Eleuthesides and their analogs: V. Medium- and large-ring lactones based on levoglucosenone. Russian Journal of Organic Chemistry. 50(1). 117–127. 20 indexed citations
14.
Валеев, Ф. А., et al.. (2014). Synthesis of α-bromoisolevoglucosenone and its cyclopenta annulation. Russian Journal of Organic Chemistry. 50(9). 1317–1322. 4 indexed citations
15.
Спирихин, Л. В., et al.. (2010). Reactions of stereocontrolled intramolecular carbocyclization of levoglucosenone adduct with isoprene. Russian Journal of Organic Chemistry. 46(2). 226–235. 6 indexed citations
16.
Валеев, Ф. А., et al.. (2004). Functionalization of the Allyl Fragment in (+)-δ-Cadinol. Russian Journal of Organic Chemistry. 40(3). 337–345. 1 indexed citations
17.
Мифтахов, М. С., et al.. (2000). Tandem transformations initiated and determined by the Michael reaction. Russian Chemical Reviews. 69(12). 1001–1019. 34 indexed citations
18.
Валеев, Ф. А., et al.. (1999). Reactions of 3-iodolevoglucosenone with sodium derivatives of some CH acids. Chiral cyclopropanes and stable oxetenes. Russian Chemical Bulletin. 48(1). 152–156. 6 indexed citations
19.
Валеев, Ф. А., et al.. (1998). Reaction of (+)-5-formyloxy-4S-chloropent-2(Z)-enonitrile with dimethyldilithiumcyanocuprate. 34(6). 937–938.
20.
Мифтахов, М. С., Ф. А. Валеев, & Irina N. Gaisina. (1994). Levoglucosenone: the properties, reactions, and use in fine organic synthesis. Russian Chemical Reviews. 63(10). 869–882. 49 indexed citations

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