É. S. Batyeva

701 total citations
105 papers, 533 citations indexed

About

É. S. Batyeva is a scholar working on Organic Chemistry, Inorganic Chemistry and Oncology. According to data from OpenAlex, É. S. Batyeva has authored 105 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 99 papers in Organic Chemistry, 10 papers in Inorganic Chemistry and 7 papers in Oncology. Recurrent topics in É. S. Batyeva's work include Synthesis and Reactivity of Sulfur-Containing Compounds (81 papers), Organophosphorus compounds synthesis (56 papers) and Organometallic Compounds Synthesis and Characterization (44 papers). É. S. Batyeva is often cited by papers focused on Synthesis and Reactivity of Sulfur-Containing Compounds (81 papers), Organophosphorus compounds synthesis (56 papers) and Organometallic Compounds Synthesis and Characterization (44 papers). É. S. Batyeva collaborates with scholars based in Russia, United States and Germany. É. S. Batyeva's co-authors include Оleg G. Sinyashin, V. A. Al’fonsov, И. С. Низамов, A. N. Pudovik, R. А. Cherkasov, А.Т. Губайдуллин, I.А. Litvinov, Olga Kataeva, Dmitry B. Krivolapov and Liliya V. Frolova and has published in prestigious journals such as Inorganic Chemistry, Corrosion Science and Journal of Organometallic Chemistry.

In The Last Decade

É. S. Batyeva

94 papers receiving 516 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
É. S. Batyeva Russia 11 423 100 65 53 53 105 533
Karim Chkirate Morocco 13 319 0.8× 158 1.6× 91 1.4× 104 2.0× 117 2.2× 40 493
Jyothi Kudva India 13 224 0.5× 78 0.8× 96 1.5× 40 0.8× 23 0.4× 30 357
Walid Guerrab Morocco 12 360 0.9× 102 1.0× 117 1.8× 75 1.4× 29 0.5× 42 505
Ali Ahmed Abdulridha Iraq 6 262 0.6× 130 1.3× 25 0.4× 72 1.4× 43 0.8× 9 411
Esvet Akbaş Türkiye 10 276 0.7× 125 1.3× 30 0.5× 88 1.7× 72 1.4× 23 424
Mehtap Yakut Türkiye 13 301 0.7× 76 0.8× 25 0.4× 42 0.8× 26 0.5× 25 395
M. Sukeri M. Yusof Malaysia 7 197 0.5× 93 0.9× 128 2.0× 51 1.0× 62 1.2× 68 347
Hamida Idan Salman Iraq 6 252 0.6× 145 1.4× 25 0.4× 80 1.5× 43 0.8× 22 408
Saqib Ali Pakistan 13 170 0.4× 97 1.0× 124 1.9× 18 0.3× 141 2.7× 33 351
Khalissa Benbouguerra Algeria 9 288 0.7× 240 2.4× 17 0.3× 165 3.1× 54 1.0× 13 523

Countries citing papers authored by É. S. Batyeva

Since Specialization
Citations

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

Fields of papers citing papers by É. S. Batyeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by É. S. Batyeva. 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 É. S. Batyeva. The network helps show where É. S. Batyeva may publish in the future.

Co-authorship network of co-authors of É. S. Batyeva

This figure shows the co-authorship network connecting the top 25 collaborators of É. S. Batyeva. A scholar is included among the top collaborators of É. S. Batyeva 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 É. S. Batyeva. É. S. Batyeva 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.
Batyeva, É. S., et al.. (2024). Proteinogenic amino acids in the synthesis of chiral salts of O, O-diterpenyl dithiophosphoric acids. Russian Chemical Bulletin. 73(3). 606–615. 1 indexed citations
2.
Низамов, И. С., et al.. (2023). Atropinium dithiophosphates and dithiophosphonates on the basis of α-D-glucofuranose and α-D-galactopyranose diacetonide scaffolds. Journal of Chemical Sciences. 135(4). 1 indexed citations
3.
Низамов, И. С., et al.. (2022). Chiral Salts of Dithiophosphonic Acids on the Basis of Monoterpenyl Alcohols and Cinchona Alkaloids. Russian Journal of General Chemistry. 92(12). 2620–2630. 1 indexed citations
4.
Низамов, И. С., et al.. (2021). Chiral salts of dithiophosphoric acids on the basis of organic nitrogen compounds. Phosphorus, sulfur, and silicon and the related elements. 197(5-6). 535–537. 1 indexed citations
5.
Batyeva, É. S., et al.. (2020). Pyridoxonium salts of chiral and cyclic dithiophosphoric and bisdithiophosphonic acids and their antimicrobial activities. Phosphorus, sulfur, and silicon and the related elements. 196(4). 431–438. 7 indexed citations
6.
Низамов, И. С., et al.. (2019). Pyridinium salts of dithiophosphoric acids on the basis of nicotinic acids and their isomers, 3-hydroxypyridine, and 3-pyridinemethanol. Phosphorus, sulfur, and silicon and the related elements. 195(3). 226–230. 4 indexed citations
7.
8.
Низамов, И. С., et al.. (2018). Chiral S‐stannyl dithiophosphates and dithiophosphonates on the basis of monoterpenols. Applied Organometallic Chemistry. 32(5). 3 indexed citations
9.
Низамов, И. С., et al.. (2018). Synthesis and characterization of pyridoxine, nicotine and nicotinamide salts of dithiophosphoric acids as antibacterial agents against resistant wound infection. Bioorganic & Medicinal Chemistry. 27(1). 100–109. 33 indexed citations
10.
Губайдуллин, А.Т., et al.. (2016). New method for the synthesis of ammonium salts of O,O'-alkylenedithiophosphoric acid and octathiotetraphosphetane. Crystal structure features's of diethylammonium salt of O,O'-propylenedithiophosphoric acid. Phosphorus, sulfur, and silicon and the related elements. 191(3). 405–410. 12 indexed citations
11.
Низамов, И. С., et al.. (2015). Dithiophosphorylation of methyl (S)-(–)-lactate. Russian Journal of Organic Chemistry. 51(7). 1026–1027. 2 indexed citations
12.
Низамов, И. С., et al.. (2014). Long-Chain Alkyl Esters of O,O-Dialkyl Dithiophosphoric and Thionophosphoric Acids Prepared on the Basis of Red Phosphorus, Elemental Sulfur, Alcohols, and Industrial Fractions of Higher Monoolefins. Phosphorus, sulfur, and silicon and the related elements. 190(4). 484–493. 2 indexed citations
13.
Низамов, И. С., et al.. (2014). Dithiophosphorylation of trimethylsilyl ethers of enantiomerically pure menthols. Russian Journal of General Chemistry. 84(12). 2467–2469. 3 indexed citations
14.
Frolova, Liliya V., et al.. (2006). Synthesis and thermal stability of S‐trimethylsilyl esters of tetracoordinated phosphorus amidothioacids. Heteroatom Chemistry. 17(7). 670–675. 2 indexed citations
15.
Губайдуллин, А.Т., et al.. (2005). Synthesis and crystal structure of the tetraalkylammonium salts of 1,2,3,4-tetramercapto-1,2,3,4-tetrathioxotetraphosphetane based on white phosphorus. Mendeleev Communications. 15(1). 22–23. 8 indexed citations
16.
Низамов, И. С., et al.. (2004). The reaction of triphenylarsine oxide with ethyl iodo‐acetate leading to triphenyl (carboethoxy)methylarsonium triiodide. Heteroatom Chemistry. 15(7). 482–485. 2 indexed citations
17.
Batyeva, É. S., et al.. (2004). Disilyl dithiophosphonates in the synthesis of open chain and cyclic organothiophosphorus compounds. Heteroatom Chemistry. 15(3). 225–232. 6 indexed citations
18.
Низамов, И. С., et al.. (2002). New methods of synthesis of boron, germanium, and tin derivatives of pentavalent phosphorus thioacids. Heteroatom Chemistry. 13(1). 27–35.
19.
Kataeva, Olga, et al.. (1995). A New Type of Coordination in Copper(I) Complexes with Trivalent Phosphorus Compounds Containing Phosphorus-Sulfur Bonds. Inorganic Chemistry. 34(21). 5171–5174. 13 indexed citations
20.
Pudovik, A. N., et al.. (1988). Acid catalysis of the reactions of n-acetoxymethylamides of benzoic and acetic acids with diethylamidodiethylphosphite. Russian Chemical Bulletin. 37(2). 389–391. 1 indexed citations

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