V. I. Galkin

1.4k total citations
107 papers, 1.2k citations indexed

About

V. I. Galkin is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, V. I. Galkin has authored 107 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Organic Chemistry, 20 papers in Inorganic Chemistry and 11 papers in Molecular Biology. Recurrent topics in V. I. Galkin's work include Organophosphorus compounds synthesis (66 papers), Phosphorus compounds and reactions (49 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (38 papers). V. I. Galkin is often cited by papers focused on Organophosphorus compounds synthesis (66 papers), Phosphorus compounds and reactions (49 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (38 papers). V. I. Galkin collaborates with scholars based in Russia, Germany and Sweden. V. I. Galkin's co-authors include R. А. Cherkasov, Yu. V. Bakhtiyarova, Artem Cherkasov, И. В. Галкина, Olga Kataeva, Daut R. Islamov, A. R. Garifzyanov, I.А. Litvinov, А.Т. Губайдуллин and Dmitry B. Krivolapov and has published in prestigious journals such as SHILAP Revista de lepidopterología, Tetrahedron Letters and Journal of Organometallic Chemistry.

In The Last Decade

V. I. Galkin

100 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. I. Galkin Russia 18 1.0k 285 158 108 103 107 1.2k
B. Sridhar India 17 636 0.6× 202 0.7× 151 1.0× 145 1.3× 231 2.2× 82 1.1k
Thomas Oeser Germany 17 977 1.0× 144 0.5× 156 1.0× 73 0.7× 155 1.5× 65 1.2k
R. А. Cherkasov Russia 21 1.8k 1.8× 647 2.3× 219 1.4× 89 0.8× 152 1.5× 270 2.2k
В. В. Ковалев Russia 17 726 0.7× 226 0.8× 179 1.1× 121 1.1× 375 3.6× 174 1.2k
B. Narayana India 19 708 0.7× 154 0.5× 72 0.5× 156 1.4× 235 2.3× 80 1.2k
H.‐J. NICLAS Germany 14 644 0.6× 145 0.5× 193 1.2× 137 1.3× 215 2.1× 75 1.1k
Uwe Huniar Germany 13 274 0.3× 200 0.7× 181 1.1× 59 0.5× 165 1.6× 16 882
Musa A. Said Saudi Arabia 22 785 0.8× 299 1.0× 84 0.5× 41 0.4× 114 1.1× 73 987
В. И. Поткин Belarus 15 815 0.8× 141 0.5× 187 1.2× 47 0.4× 119 1.2× 198 1.0k
Belén Rodrı́guez Germany 10 864 0.9× 215 0.8× 286 1.8× 153 1.4× 135 1.3× 12 1.1k

Countries citing papers authored by V. I. Galkin

Since Specialization
Citations

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

Fields of papers citing papers by V. I. Galkin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. I. Galkin. 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 V. I. Galkin. The network helps show where V. I. Galkin may publish in the future.

Co-authorship network of co-authors of V. I. Galkin

This figure shows the co-authorship network connecting the top 25 collaborators of V. I. Galkin. A scholar is included among the top collaborators of V. I. Galkin 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 V. I. Galkin. V. I. Galkin 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.
Герасимов, А. В., et al.. (2022). Reactions of Triphenylphospine with ω-Bromoalkanecarboxylic Acids. Russian Journal of General Chemistry. 92(7). 1214–1220. 5 indexed citations
2.
Bakhtiyarova, Yu. V., et al.. (2021). Carboxylate Phosphabetaines Containing Chiral Carbon Atom: Synthesis and NMR Spectroscopy Data. Russian Journal of General Chemistry. 91(7). 1333–1341. 6 indexed citations
3.
Bakhtiyarova, Yu. V., et al.. (2019). Synthesis, structure and bioactivity of novel carboxylate phosphabetaine derivatives with long alkyl chains. Phosphorus, sulfur, and silicon and the related elements. 194(4-6). 476–479. 8 indexed citations
4.
Bakhtiyarova, Yu. V., et al.. (2018). The reaction of phosphorylation of trans-aconitic acid by tertiary phosphines. Phosphorus, sulfur, and silicon and the related elements. 194(4-6). 319–320. 6 indexed citations
5.
Галкина, И. В., et al.. (2016). Synthesis and biological evaluation of novel carboxylate phosphabetaines derivatives with long alkyl chains. Phosphorus, sulfur, and silicon and the related elements. 191(11-12). 1676–1678. 7 indexed citations
6.
Bakhtiyarova, Yu. V., et al.. (2016). New di- and tricarboxylate phosphabetaines. Russian Chemical Bulletin. 65(5). 1308–1312. 12 indexed citations
7.
Bakhtiyarova, Yu. V., et al.. (2015). Synthesis of carboxylate arsenobetaines based on (carboxyalkyl)triphenylarsonium halides. Russian Journal of General Chemistry. 85(9). 2058–2064. 3 indexed citations
8.
Галкина, И. В., et al.. (2014). Synthesis and Antimicrobial Activity of Bis-4,6-sulfonamidated 5,7-Dinitrobenzofuroxans. Journal of Chemistry. 2014. 1–6. 16 indexed citations
9.
Галкина, И. В., et al.. (2012). Synthesis and Antimicrobial Activities of Phosphonium Salts on Basis of Triphenylphosphine and 3,5-Di-Tert-Butyl-4-Hydroxybenzyl Bromide. Phosphorus, sulfur, and silicon and the related elements. 188(1-3). 15–18. 16 indexed citations
10.
Bakhtiyarova, Yu. V., et al.. (2012). Synthesis of quaternary phosphonium salts from phosphorylated sterically hindered phenols. Russian Journal of Organic Chemistry. 48(12). 1574–1575. 4 indexed citations
11.
Bakhtiyarova, Yu. V., et al.. (2010). Kinetic study of the reaction of triphenylphosphine with acrylic acid in alcohol media. Russian Journal of General Chemistry. 80(9). 1738–1742. 14 indexed citations
12.
Galkin, V. I., et al.. (2009). Kinetics and mechanism of triphenylphosphine quarternization with unsaturated carboxylic acids in the medium of acetic acid. Russian Journal of General Chemistry. 79(5). 919–924. 22 indexed citations
13.
Галкина, И. В., et al.. (2009). An Unusual Reaction of Triphenylphosphine with Dichlorodinitrobenzofuroxan. Phosphorus, sulfur, and silicon and the related elements. 184(4). 987–991. 11 indexed citations
14.
Garifzyanov, A. R., et al.. (2005). Liquid Extraction of Noble Metal Ions with an α-Amino Phosphonate. Russian Journal of General Chemistry. 75(8). 1208–1211. 19 indexed citations
15.
Garifzyanov, A. R., et al.. (2004). Synthesis and Acid-Base Properties of α-Aminophosphoryl Compounds. Russian Journal of General Chemistry. 74(6). 873–881. 22 indexed citations
16.
Kaļiņina, Irina, et al.. (2004). Esterification of Phosphorus Electrophiles with 3,4-Dichloro-5-hydroxyfuran-2(5H-one. Russian Journal of Organic Chemistry. 40(3). 438–440.
17.
Миронов, В. Ф., et al.. (2004). Theoretical and Experimental Investigation of Reactions between Dialkyl Phosphites and tert-Butylphosphaethyne. Russian Journal of Organic Chemistry. 40(8). 1076–1079. 1 indexed citations
18.
Galkin, V. I., et al.. (1999). Kinetics and Mechanism of the Insertion Reaction of Arylisocyanates into C‒C Bond of Phosphabetaine Obtained ont the Basis of Triisopropylphosphine and 2-Cyanoethylacrylate. Phosphorus, sulfur, and silicon and the related elements. 147(1). 89–89. 1 indexed citations
19.
Galkin, V. I., et al.. (1995). The primary zone in the combustion of solid propellants containing catalysts. Combustion Explosion and Shock Waves. 31(2). 161–167. 21 indexed citations
20.
Galkin, V. I., et al.. (1987). Acid properties of dialkyl phosphites and their reactivity in the reaction with benzalacetophenone. 32(1). 273–85. 1 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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