В. В. Липсон

1.2k total citations
80 papers, 896 citations indexed

About

В. В. Липсон is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, В. В. Липсон has authored 80 papers receiving a total of 896 indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Organic Chemistry, 15 papers in Molecular Biology and 5 papers in Pharmacology. Recurrent topics in В. В. Липсон's work include Synthesis and Characterization of Heterocyclic Compounds (42 papers), Synthesis and biological activity (24 papers) and Synthesis and Reactions of Organic Compounds (19 papers). В. В. Липсон is often cited by papers focused on Synthesis and Characterization of Heterocyclic Compounds (42 papers), Synthesis and biological activity (24 papers) and Synthesis and Reactions of Organic Compounds (19 papers). В. В. Липсон collaborates with scholars based in Ukraine, Russia and United Kingdom. В. В. Липсон's co-authors include Tetiana Pavlovska, Ruslan Gr. Redkin, Sergey M. Desenko, Олег В. Шишкин, Svitlana V. Shishkina, Владимир И. Мусатов, Nikolay Yu. Gorobets, В. Д. Орлов, Yu. T. Struchkov and A.V. Borisov and has published in prestigious journals such as Tetrahedron, New Journal of Chemistry and Journal of Molecular Structure.

In The Last Decade

В. В. Липсон

73 papers receiving 876 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
В. В. Липсон Ukraine 13 832 148 56 34 23 80 896
Владимир И. Мусатов Ukraine 15 843 1.0× 182 1.2× 66 1.2× 24 0.7× 15 0.7× 94 892
Ravindra M. Kumbhare India 16 707 0.8× 228 1.5× 33 0.6× 33 1.0× 12 0.5× 38 812
Diana Becerra Colombia 13 633 0.8× 125 0.8× 75 1.3× 11 0.3× 20 0.9× 37 716
Sarbjot Singh India 5 350 0.4× 97 0.7× 43 0.8× 32 0.9× 9 0.4× 12 469
Abdelali Kerbal Morocco 14 550 0.7× 144 1.0× 61 1.1× 14 0.4× 16 0.7× 71 657
Sindu Ros Italy 12 415 0.5× 227 1.5× 79 1.4× 19 0.6× 8 0.3× 16 596
A. HERCOUET France 16 553 0.7× 151 1.0× 58 1.0× 53 1.6× 10 0.4× 36 624
T. V. Sravanthi India 4 542 0.7× 100 0.7× 37 0.7× 28 0.8× 6 0.3× 7 623
Hend N. Hafez Egypt 18 1.1k 1.4× 209 1.4× 107 1.9× 9 0.3× 16 0.7× 38 1.2k
Sumit S. Chourasiya India 14 382 0.5× 141 1.0× 26 0.5× 20 0.6× 7 0.3× 20 476

Countries citing papers authored by В. В. Липсон

Since Specialization
Citations

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

Fields of papers citing papers by В. В. Липсон

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by В. В. Липсон. 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 В. В. Липсон. The network helps show where В. В. Липсон may publish in the future.

Co-authorship network of co-authors of В. В. Липсон

This figure shows the co-authorship network connecting the top 25 collaborators of В. В. Липсон. A scholar is included among the top collaborators of В. В. Липсон 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 В. В. Липсон. В. В. Липсон 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.
Липсон, В. В., et al.. (2024). Discovery of Novel N-Acylhydrazone Derivatives as Potent Inhibitors of Sirtuin-1. SynOpen. 8(2). 100–108. 2 indexed citations
2.
Чебанов, Валентин А., Sergey M. Desenko, & В. В. Липсон. (2023). Heterocycles on the crest of microwaves and ultrasonics in the Institute for Single Crystals of National Academy of Sciences of Ukraine: chemistry and history. Chemistry of Heterocyclic Compounds. 59(6-7). 386–405. 2 indexed citations
3.
Pavlovska, Tetiana, A. Kolomiets, Владимир И. Мусатов, et al.. (2023). Effective Three‐Step Construction of Betulonic Acid Hybrids with Heterocycle‐Containing Peptidomimetic Fragments. ChemistrySelect. 8(27). 2 indexed citations
4.
Desenko, Sergey M., Nikolay Yu. Gorobets, В. В. Липсон, Yana I. Sakhno, & Валентин А. Чебанов. (2023). Dihydroazolopyrimidines: Past, Present and Perspectives in Synthesis, Green Chemistry and Drug Discovery. The Chemical Record. 24(2). e202300244–e202300244. 8 indexed citations
5.
6.
Липсон, В. В., et al.. (2023). Synthesis of methotrexate-betulonic acid hybrids and evaluation of their effect on artificial and Caco-2 cell membranes. Steroids. 201. 109332–109332. 1 indexed citations
7.
Липсон, В. В., Tetiana Pavlovska, Nikolay Yu. Gorobets, et al.. (2019). Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-c]imidazoles via the domino reactions of 2-amino-4-arylimidazoles with carbonyl and methylene active compounds. Beilstein Journal of Organic Chemistry. 15. 1032–1045. 4 indexed citations
8.
Pavlovska, Tetiana, В. В. Липсон, Svitlana V. Shishkina, et al.. (2019). 1,3-Dipolar cycloaddition of (E)-4-(4-chlorophenyl)-2-oxobut-3-enic acid to 2-oxindole azomethine ylides. Chemistry of Heterocyclic Compounds. 55(7). 679–683. 3 indexed citations
9.
10.
Shishkina, Svitlana V., et al.. (2016). Chemical transformations of betulonic aldehyde. Russian Journal of Organic Chemistry. 52(2). 249–260. 7 indexed citations
11.
Pavlovska, Tetiana, et al.. (2015). Molecular diversity of spirooxindoles. Synthesis and biological activity. Molecular Diversity. 20(1). 299–344. 300 indexed citations
12.
Shishkina, Svitlana V., et al.. (2015). 3+2-Dipolar cycloaddition of dianhydrohexitol azidoderivatives with N-arylmaleimides. Journal of Molecular Structure. 1100. 384–394. 2 indexed citations
13.
14.
Redkin, Ruslan Gr., et al.. (2013). SYNTHESIS AND CHEMICAL PROPERTIES OF NEW DERIVATIVES OF 3a',6a'-DIHYDRO-2' H -SPIRO[INDOLE-3,1'-PYRROLO[3,4- c ]PYRROLE]2,4',6'(1 H ,3' H ,5' H )-TRIONE. Chemistry of Heterocyclic Compounds. 945–960. 1 indexed citations
15.
Липсон, В. В. & Nikolay Yu. Gorobets. (2009). One hundred years of Meldrum’s acid: advances in the synthesis of pyridine and pyrimidine derivatives. Molecular Diversity. 13(4). 399–419. 64 indexed citations
16.
Липсон, В. В., et al.. (2007). Synthesis and tautomerism of 5,7-diaryl-3-cyano-and 5,7-diaryl-3-ethoxycarbonyl-4,7(6,7)-dihydropyrazolo[1,5-a]pyrimidines. Chemistry of Heterocyclic Compounds. 43(12). 1544–1550. 6 indexed citations
17.
Липсон, В. В., et al.. (2005). 2-Methylthio-4,5,6,7-tetrahydro-1,2,4-triazolo[1,5-a]pyrimidin-5- and -7-Ones. Chemistry of Heterocyclic Compounds. 41(2). 216–220. 6 indexed citations
18.
19.
Desenko, Sergey M., Олег В. Шишкин, В. Д. Орлов, et al.. (1994). Synthesis and structure of 4,5,6,7-tetrahydro-1,2,4-triazolo[1,5-a]pyrimidines. Chemistry of Heterocyclic Compounds. 30(7). 851–855. 7 indexed citations
20.
Lindeman, S.V., et al.. (1993). Structure of 2-methyl-5,6,7-triphenyl-6,7-dihydropyrazolo[2,3-a]pyrimidine. Acta Crystallographica Section C Crystal Structure Communications. 49(5). 896–898. 3 indexed citations

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