G. A. Panosyan

600 total citations
137 papers, 414 citations indexed

About

G. A. Panosyan is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, G. A. Panosyan has authored 137 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 123 papers in Organic Chemistry, 20 papers in Pharmaceutical Science and 16 papers in Molecular Biology. Recurrent topics in G. A. Panosyan's work include Synthesis and Reactions of Organic Compounds (49 papers), Synthesis and Characterization of Heterocyclic Compounds (32 papers) and Synthesis and biological activity (22 papers). G. A. Panosyan is often cited by papers focused on Synthesis and Reactions of Organic Compounds (49 papers), Synthesis and Characterization of Heterocyclic Compounds (32 papers) and Synthesis and biological activity (22 papers). G. A. Panosyan collaborates with scholars based in Armenia, Russia and United States. G. A. Panosyan's co-authors include P. V. Petrovskii, V. N. Setkina, D. N. Kursanov, A. G. Ginzburg, R. А. Tamazyan, N. E. Kolobova, N. I. Vasyukova, M. I. Rybinskaya, V. V. Krivykh and E.I. Fedin and has published in prestigious journals such as Journal of Organometallic Chemistry, Russian Journal of Plant Physiology and Russian Chemical Bulletin.

In The Last Decade

G. A. Panosyan

114 papers receiving 385 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. A. Panosyan Armenia 11 376 59 31 30 26 137 414
Yury S. Halauko Belarus 16 526 1.4× 67 1.1× 57 1.8× 29 1.0× 16 0.6× 28 568
Petra Böhrer Germany 11 353 0.9× 90 1.5× 36 1.2× 13 0.4× 52 2.0× 29 412
Tatyana N. Borodina Russia 12 320 0.9× 56 0.9× 26 0.8× 30 1.0× 12 0.5× 55 380
James R. Matz United States 12 388 1.0× 72 1.2× 54 1.7× 21 0.7× 32 1.2× 15 451
Osamu Niyomura Japan 14 490 1.3× 193 3.3× 41 1.3× 24 0.8× 23 0.9× 29 554
Olesya V. Khoroshilova Russia 13 330 0.9× 65 1.1× 53 1.7× 12 0.4× 33 1.3× 44 399
Ghenia Bentabed‐Ababsa France 18 683 1.8× 73 1.2× 90 2.9× 19 0.6× 9 0.3× 34 729
Michael Duetsch Germany 14 833 2.2× 149 2.5× 42 1.4× 27 0.9× 26 1.0× 19 873
Andrée Parlier France 17 673 1.8× 102 1.7× 41 1.3× 14 0.5× 22 0.8× 46 715
Tadeusz S. Jagodziński Poland 9 603 1.6× 31 0.5× 64 2.1× 9 0.3× 30 1.2× 32 641

Countries citing papers authored by G. A. Panosyan

Since Specialization
Citations

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

Fields of papers citing papers by G. A. Panosyan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. A. Panosyan. 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 G. A. Panosyan. The network helps show where G. A. Panosyan may publish in the future.

Co-authorship network of co-authors of G. A. Panosyan

This figure shows the co-authorship network connecting the top 25 collaborators of G. A. Panosyan. A scholar is included among the top collaborators of G. A. Panosyan 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 G. A. Panosyan. G. A. Panosyan 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.
Panosyan, G. A., et al.. (2020). Synthesis and Antitumor Activity of Piperazine-Based Tertiary Amino Alcohols and Their Dihydrochlorides. Russian Journal of General Chemistry. 90(6). 1088–1092. 1 indexed citations
2.
Panosyan, G. A., et al.. (2017). Synthesis of β-amino ketones derived from aminobenzoic acids. Russian Journal of General Chemistry. 87(2). 342–346. 1 indexed citations
3.
Panosyan, G. A., et al.. (2015). Synthesis and properties of new benzo[4,5]thiazolo[3,2-a]pyrimidine derivatives. Russian Journal of Organic Chemistry. 51(5). 711–714. 8 indexed citations
4.
Panosyan, G. A., et al.. (2014). Synthesis and estimation of antibacterial activity of 3-(4-butoxyphenyl)- and 3-[4-(3-methylbutoxy)phenyl]-1-(morpholin-4-yl)-2-phenylalkan-3-ols hydrochlorides. Russian Journal of Organic Chemistry. 50(8). 1203–1206. 1 indexed citations
5.
6.
Panosyan, G. A., et al.. (2007). Reaction of triphenyl(phenylethynyl)phosphonium bromide with α-aminoethers, dipiperidinomethane, and secondary amines. Russian Journal of General Chemistry. 77(5). 866–870. 3 indexed citations
7.
Panosyan, G. A., et al.. (2007). Derivatives of α,β-dehydro amino acids: II. New synthesis of 2,4-disubstituted 1-aminoimidazol-5-ones from N-substituted α,β-unsaturated α-amino acid hydrazides. Russian Journal of Organic Chemistry. 43(6). 936–937. 6 indexed citations
8.
Panosyan, G. A., et al.. (2005). Noncatalytic O-Alkylation of Alcohols with Pyrazolylcarbonyls. Russian Journal of General Chemistry. 75(9). 1500–1501. 3 indexed citations
9.
Panosyan, G. A., et al.. (2005). Synthesis and Some Transformations of 2-(3-Amino-1-Phenylpropyl)furan. Chemistry of Heterocyclic Compounds. 41(4). 437–441. 1 indexed citations
10.
Panosyan, G. A., et al.. (2005). Alkylation of 3,4-Dibromo-4-methyltetrahydropyran with Diethyl Malonate as a Key to Understanding the Electronic Nature of Chemo- and Regioselectivity of Molecules. Russian Journal of Organic Chemistry. 41(1). 134–140. 2 indexed citations
11.
Panosyan, G. A., et al.. (2005). Synthesis of 1,4-Bis(dimethylamino)-2,3-dibromo-2-butene and Its Quaternary Derivatives. Russian Journal of General Chemistry. 75(5). 724–726. 2 indexed citations
12.
Panosyan, G. A., et al.. (2004). Cyclodimerization of the Stevens Rearrangement Products from 4-Alkoxy-2-butynyl(alkoxycarbonylmethyl)dimethyl-ammonium Salts into Cyclohexene Derivatives. Russian Journal of Organic Chemistry. 40(7). 936–939. 1 indexed citations
13.
Panosyan, G. A., et al.. (2004). Synthesis and Heterocyclization of β-Aroyl-α-diphenylphosphorylpropionic Acids. Chemistry of Heterocyclic Compounds. 40(4). 446–451. 3 indexed citations
14.
Parsadanyan, Marine A., et al.. (2000). Changes in the nucleotide composition and pattern of DNA methylation during the germination of cereal seeds.. Russian Journal of Plant Physiology. 47(2). 256–259. 1 indexed citations
15.
Panosyan, G. A., et al.. (1987). Structure of the proton skeleton of nitrobenzene, determined by1H NMR in the nematic phase. Journal of Structural Chemistry. 28(2). 318–321. 1 indexed citations
16.
17.
Panosyan, G. A., et al.. (1981). Reactions of 1-halo-3-methyl-2,3-epoxybutane with alcohols. Chemistry of Heterocyclic Compounds. 17(7). 642–644.
18.
Fedorov, L. A., et al.. (1979). The 13C NMR spectra of π-arenechromium carbonyl complexes. Journal of Organometallic Chemistry. 182(4). 499–510. 18 indexed citations
19.
Ginzburg, A. G., et al.. (1976). Metallocenyl cations. Journal of Organometallic Chemistry. 121(3). 381–389. 10 indexed citations
20.
Ginzburg, A. G., et al.. (1974). Protonation of metal carbonyl complexes. Journal of Organometallic Chemistry. 81(2). 201–205. 24 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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