А. Е. Рубцов

1.1k total citations
71 papers, 895 citations indexed

About

А. Е. Рубцов is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, А. Е. Рубцов has authored 71 papers receiving a total of 895 indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Organic Chemistry, 4 papers in Inorganic Chemistry and 3 papers in Molecular Biology. Recurrent topics in А. Е. Рубцов's work include Chemical synthesis and pharmacological studies (40 papers), Synthesis and Reactions of Organic Compounds (23 papers) and Synthesis of heterocyclic compounds (15 papers). А. Е. Рубцов is often cited by papers focused on Chemical synthesis and pharmacological studies (40 papers), Synthesis and Reactions of Organic Compounds (23 papers) and Synthesis of heterocyclic compounds (15 papers). А. Е. Рубцов collaborates with scholars based in Russia, United Kingdom and United States. А. Е. Рубцов's co-authors include Sergei A. Shipilovskikh, Andrei V. Malkov, Р. Р. Махмудов, Н. М. Игидов, D. A. Shipilovskikh, Антон С. Макаров, А. В. Бутин, Vladimir Gevorgyan, Celia A. Incerti‐Pradillos and Mikhail Kabeshov and has published in prestigious journals such as SHILAP Revista de lepidopterología, Green Chemistry and The Journal of Organic Chemistry.

In The Last Decade

А. Е. Рубцов

70 papers receiving 888 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
А. Е. Рубцов Russia 20 826 76 51 23 21 71 895
Vipan Kumar India 15 483 0.6× 85 1.1× 43 0.8× 31 1.3× 26 1.2× 32 550
Sumit S. Chourasiya India 14 382 0.5× 141 1.9× 42 0.8× 33 1.4× 26 1.2× 20 476
Ashok Kumar Yadav India 16 633 0.8× 103 1.4× 42 0.8× 21 0.9× 19 0.9× 39 691
İlhan Işıkdağ Türkiye 8 610 0.7× 139 1.8× 31 0.6× 31 1.3× 39 1.9× 21 703
Chennan Ramalingan India 13 502 0.6× 172 2.3× 78 1.5× 37 1.6× 25 1.2× 27 580
Neal J. Fazakerley United Kingdom 9 598 0.7× 94 1.2× 99 1.9× 36 1.6× 36 1.7× 11 704
Habibe Erdeniz Türkiye 7 528 0.6× 96 1.3× 47 0.9× 23 1.0× 42 2.0× 11 585
S. Amirthaganesan India 9 289 0.3× 89 1.2× 42 0.8× 43 1.9× 21 1.0× 20 390
Hassan A. El‐Sayed Egypt 17 655 0.8× 110 1.4× 26 0.5× 49 2.1× 23 1.1× 69 749
B. Sooryanarayana Rao India 10 895 1.1× 128 1.7× 46 0.9× 22 1.0× 41 2.0× 15 961

Countries citing papers authored by А. Е. Рубцов

Since Specialization
Citations

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

Fields of papers citing papers by А. Е. Рубцов

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of А. Е. Рубцов

This figure shows the co-authorship network connecting the top 25 collaborators of А. Е. Рубцов. A scholar is included among the top collaborators of А. Е. Рубцов 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 А. Е. Рубцов. А. Е. Рубцов 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.
Karpov, Timofey E., А. Е. Рубцов, D. A. Shipilovskikh, et al.. (2023). Synthesis of thieno[3,2-e]pyrrolo[1,2-a]pyrimidine derivatives and their precursors containing 2-aminothiophenes fragments as anticancer agents for therapy of pulmonary metastatic melanoma. European Journal of Medicinal Chemistry. 254. 115325–115325. 29 indexed citations
2.
Burykina, Julia V., Артем Н. Фахрутдинов, Felix Plasser, et al.. (2023). Mechanistic Insight into Palladium‐Catalyzed Asymmetric Alkylation of Indoles with Diazoesters Employing Bipyridine‐N,N’‐dioxides as Chiral Controllers. Advanced Synthesis & Catalysis. 366(1). 121–133. 2 indexed citations
3.
Du, Yi, et al.. (2023). Catalytic prenylation of natural polyphenols. New Journal of Chemistry. 47(44). 20358–20362. 2 indexed citations
4.
5.
Shipilovskikh, D. A., Р. Р. Махмудов, А. Е. Рубцов, & Sergei A. Shipilovskikh. (2021). Hydrolysis of Substituted 3-(Thien-2-yl)imino-3H-furan-2-ones and Anti-Inflammatory Activity of the Reaction Products. Russian Journal of General Chemistry. 91(10). 2025–2030. 4 indexed citations
6.
Malkov, Andrei V. & А. Е. Рубцов. (2021). Developing a Methodology for Catalytic Asymmetric Crotylation of Aldehydes. Synlett. 32(14). 1397–1405. 2 indexed citations
7.
Ткаченко, А. Г., et al.. (2021). A synthetic diterpene analogue inhibits mycobacterial persistence and biofilm formation by targeting (p)ppGpp synthetases. Cell chemical biology. 28(10). 1420–1432.e9. 21 indexed citations
8.
Ткаченко, А. Г., et al.. (2020). A Novel Synthetic Diterpene Reduces Mycobacterial Persistence and Biofilm Formation by Targeting (p)ppGpp Synthetases. SSRN Electronic Journal. 2 indexed citations
9.
Shipilovskikh, Sergei A., et al.. (2020). Synthesis and Antinociceptive Activity of N-Substituted 4-Aryl-4-oxo-2-[(3-thiophen-2-yl)amino]but-2-enamides. Russian Journal of General Chemistry. 90(4). 583–589. 16 indexed citations
10.
Shipilovskikh, Sergei A., et al.. (2019). Stereoselective Synthesis of Atropisomeric Bipyridine N,N′-Dioxides by Oxidative Coupling. Organic Letters. 21(12). 4798–4802. 21 indexed citations
11.
Махмудов, Р. Р., et al.. (2018). Synthesis and Biological Activity of 4-ARYL-2-[(2-OXO-1,2-Diphenylethylidene)-Hydrazinyl]-4-Oxobut-2-Enoic-Acid Amides. Pharmaceutical Chemistry Journal. 52(5). 415–418. 6 indexed citations
12.
Рубцов, А. Е., et al.. (2016). Chemistry of iminofurans: XII.1 Synthesis of 2-(arylimino)furan-3(2H)-ones and their reaction with amines. Russian Journal of Organic Chemistry. 52(6). 848–856. 2 indexed citations
13.
Рубцов, А. Е., et al.. (2016). Oxidative Azo–Ene Cyclization. Organic Letters. 19(1). 234–237. 10 indexed citations
14.
Игидов, Н. М., et al.. (2016). Chemistry of iminofurans: XI. Synthesis, structure, and cyclization of 4-substituted 2-(aroylhydrazinylidene)-4-oxobutanoic acids. Russian Journal of Organic Chemistry. 52(4). 526–532. 8 indexed citations
15.
Incerti‐Pradillos, Celia A., Mikhail Kabeshov, Sergei A. Shipilovskikh, et al.. (2015). Catalytic Asymmetric Crotylation of Aldehydes: Application in Total Synthesis of (−)‐Elisabethadione. Chemistry - A European Journal. 21(12). 4551–4555. 25 indexed citations
16.
Shipilovskikh, Sergei A. & А. Е. Рубцов. (2014). Chemistry of iminofurans. Recyclization of ethyl 2-[2-oxo-5-phenylfuran-3(2H)-ylideneamino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate by the action of hydrazines. Russian Journal of Organic Chemistry. 50(12). 1853–1855. 18 indexed citations
17.
Shipilovskikh, Sergei A. & А. Е. Рубцов. (2014). Decyclization of-2-[5-(4-chlorophenyl)-2-oxofuran-3(2H)-ylideneamino]-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide upon treatment with aliphatic alcohols. Russian Chemical Bulletin. 63(9). 2205–2207. 24 indexed citations
18.
Игидов, Н. М., et al.. (2011). Chemistry of iminofurans: VI.* Synthesis and structure of 2-(2-ylidenehydrazino)-substituted 4-aryl-4-oxobut-2-enoic and 5,5-dimethyl-4-oxohex-2-enoic acids. Russian Journal of Organic Chemistry. 47(1). 109–114. 10 indexed citations
19.
Рубцов, А. Е., et al.. (2007). Chemistry of iminofurans. Wittig reaction of 5-aryl-3-methylidenehydrazono-2,3-dihydrofuran-2-ones. Russian Journal of Organic Chemistry. 43(9). 1415–1416. 9 indexed citations
20.
Рубцов, А. Е., et al.. (2003). Synthesis and Intramolecular Cyclization of N-Substituted 2-Amino-4-aryl-4-oxo-2-butenoic Acids. Russian Journal of Organic Chemistry. 39(6). 869–874. 18 indexed citations

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