V. A. Sukach

466 total citations
51 papers, 361 citations indexed

About

V. A. Sukach is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, V. A. Sukach has authored 51 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Organic Chemistry, 17 papers in Pharmaceutical Science and 11 papers in Molecular Biology. Recurrent topics in V. A. Sukach's work include Synthesis and Reactions of Organic Compounds (26 papers), Fluorine in Organic Chemistry (17 papers) and Synthesis of heterocyclic compounds (14 papers). V. A. Sukach is often cited by papers focused on Synthesis and Reactions of Organic Compounds (26 papers), Fluorine in Organic Chemistry (17 papers) and Synthesis of heterocyclic compounds (14 papers). V. A. Sukach collaborates with scholars based in Ukraine, France and United States. V. A. Sukach's co-authors include М. В. Вовк, Эдуард Б. Русанов, V. V. Pirozhenko, Gerd‐Volker Röschenthaler, Oleksandr Maximyuk, Oleg Krishtal, Tian‐Le Xu, Dmytro Isaev, Wei‐Guang Li and Chen Huang and has published in prestigious journals such as Scientific Reports, Journal of Medicinal Chemistry and Tetrahedron.

In The Last Decade

V. A. Sukach

46 papers receiving 357 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
V. A. Sukach Ukraine	10	277	146	102	29	28	51	361
Yuji Kazuta Japan	12	276 1.0×	163 1.1×	22 0.2×	14 0.5×	29 1.0×	19	396
Antonio Vong United Kingdom	12	248 0.9×	239 1.6×	88 0.9×	11 0.4×	166 5.9×	21	495
Sandra L. Moon United States	5	260 0.9×	126 0.9×	16 0.2×	38 1.3×	75 2.7×	12	392
Peter J. Diel Switzerland	9	356 1.3×	117 0.8×	31 0.3×	87 3.0×	86 3.1×	14	482
Shuai Xu China	15	640 2.3×	76 0.5×	79 0.8×	57 2.0×	27 1.0×	22	723
Dietrich Strub Switzerland	5	140 0.5×	194 1.3×	22 0.2×	53 1.8×	184 6.6×	6	376
Matthias V. Westphal Switzerland	7	264 1.0×	193 1.3×	82 0.8×	27 0.9×	98 3.5×	11	496
Iván Collado Spain	13	289 1.0×	259 1.8×	27 0.3×	28 1.0×	86 3.1×	17	447
Silvia Bartolucci Italy	11	280 1.0×	142 1.0×	17 0.2×	94 3.2×	20 0.7×	18	374
Phong Truong United States	11	267 1.0×	59 0.4×	29 0.3×	42 1.4×	57 2.0×	26	412

Countries citing papers authored by V. A. Sukach

Since Specialization

Citations

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

Fields of papers citing papers by V. A. Sukach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. A. Sukach

This figure shows the co-authorship network connecting the top 25 collaborators of V. A. Sukach. A scholar is included among the top collaborators of V. A. Sukach 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. A. Sukach. V. A. Sukach is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ryabukhin, Sergey V., et al.. (2025). Recent advances in the photocatalytic Giese reaction. Current Chemistry Letters. 15(1). 77–100. 1 indexed citations

Shishkina, Svitlana V., et al.. (2023). Hydroaminoalkyl Functionalization of Pyrimidin‐2(1H)‐ones by Visible Light Organophotocatalysis: A Radical Approach to Biginelli‐Type Dihydropyrimidines. Advanced Synthesis & Catalysis. 365(20). 3484–3492. 3 indexed citations

Вовк, М. В., et al.. (2020). Chan–Evans–Lam N1-(het)arylation and N1-alkеnylation of 4-fluoroalkylpyrimidin-2(1H)-ones. Beilstein Journal of Organic Chemistry. 16. 2304–2313. 5 indexed citations

Sukach, V. A., et al.. (2020). Recent Achievements in Nucleophilic Decarboxylative Addition Reactions. Current Organic Chemistry. 24(19). 2193–2215. 2 indexed citations

Sukach, V. A., et al.. (2019). Access to Unprotected β-Fluoroalkyl β-Amino Acids and Their α-Hydroxy Derivatives. Organic Letters. 21(7). 2340–2345. 13 indexed citations

Shishkina, Svitlana V., et al.. (2017). Regioselective decarboxylative addition of malonic acid and its mono(thio)esters to 4-trifluoromethylpyrimidin-2(1H)-ones. Beilstein Journal of Organic Chemistry. 13. 2617–2625. 7 indexed citations

Sukach, V. A., et al.. (2017). The addition of β-ketoacids to 4-(trifluoromethyl)pyrimidin- 2(1Н)-ones with decarboxylation: an effective method for the synthesis of 4-(2-oxoalkyl)-6-(trifluoromethyl)-3,4-dihydropyrimidin-2-ones. Chemistry of Heterocyclic Compounds. 53(10). 1124–1127. 4 indexed citations

Li, Wei‐Guang, Yan‐Jiao Wu, Chen Huang, et al.. (2016). Acid-sensing ion channel 1a contributes to hippocampal LTP inducibility through multiple mechanisms. Scientific Reports. 6(1). 23350–23350. 39 indexed citations

Sukach, V. A., et al.. (2016). The synthesis and reactions of diacethyl(dialkoxycarbonyl) substituted hydroxycyclohexanones / A.I.Ismiyev, A.M.Maherramov, V.A.Sukach, M.V.Vovk. 14(4(56)). 16–32. 1 indexed citations

10.

Sukach, V. A., Veronika M. Shoba, V. V. Pirozhenko, et al.. (2014). Control of Regio‐ and Enantioselectivity in the Asymmetric Organocatalytic Addition of Acetone to 4‐(Trifluoromethyl)pyrimidin‐2(1H)‐ones. European Journal of Organic Chemistry. 2014(7). 1452–1460. 14 indexed citations

11.

Sukach, V. A., et al.. (2012). (3-carboxamidino-2-oxo-2H-chromen-7-yl)-4-guanidinobenzoates are novel blockers of pH-sensitive ion channels. Fìzìologìčnij žurnal. 57(6). 31–37. 2 indexed citations

12.

Sukach, V. A., et al.. (2012). Heterocyclization of N-(1-chloro-2,2,2-trifluoroethylidene)carbamates with β-enaminoesters—a novel synthetic strategy to functionalized trifluoromethylated pyrimidines. Tetrahedron. 68(40). 8408–8415. 25 indexed citations

13.

Sukach, V. A., et al.. (2010). Reaction of (S)-(+)-4-amino-4-aryl-5,5,5-trifluoropentan-2-ones with α-chlorobenzyl isocyanates. Synthesis of (S)-(+)-4-aryl-6-(2-arylethenyl)-4-trifluoromethyl-3,4-dihydro-pyrimidin-2(1H)-ones. Russian Journal of Organic Chemistry. 46(10). 1571–1574.

14.

Sukach, V. A., et al.. (2008). Convenient enantioselective synthesis of β-trifluoromethyl-β-aminoketones by organocatalytic asymmetric Mannich reaction of aryl trifluoromethyl ketimines with acetone. Tetrahedron Asymmetry. 19(6). 761–764. 79 indexed citations

15.

Biitseva, Angelina V., et al.. (2008). Regioselective synthesis of 4-aryl-3,4-dihydro-1,3,5-triazino[2,1-a]isoindol-2-ones. Monatshefte für Chemie - Chemical Monthly. 139(8). 939–943. 4 indexed citations

16.

Sukach, V. A., et al.. (2007). Synthesis of Novel Functionalized Derivatives of 5‐Nitro‐3,4‐dihydropyrimidin‐2(1H)‐one by the Cyclocondensation of 1‐Chlorobenzyl Isocyanates with N,S‐ and N,N‐Nitroketeneacetals.. ChemInform. 38(30). 1 indexed citations

17.

Sukach, V. A., et al.. (2007). Heterocyclization of functionalized heterocumulenes with C,N-and C,O-binucleophiles: VI. Synthesis of carbofused 2,3-dihydro-1,3-oxazin-4-ones and 3,4-dihydro-1,3-oxazin-2-ones. Russian Journal of Organic Chemistry. 43(2). 256–262. 5 indexed citations

18.

Sukach, V. A., et al.. (2006). Synthesis of functionalized 2,3-dihydrothieno[2,3-d]pyrimidin-4(1H)-ones and their recyclization to 2,3-dihydrothieno[3,4-d]pyrimidin-4(1H)-ones. Heteroatom Chemistry. 17(2). 104–111. 4 indexed citations

19.

Sukach, V. A., et al.. (2005). Synthesis of 2,3‐Dihydro‐1,3‐thiazin‐4(1H)‐ones and Their Remarkably Facile Recyclization to 2,3‐Dihydropyrimidin‐4(1H)‐ones.. ChemInform. 36(47). 1 indexed citations

20.

Sukach, V. A., et al.. (2003). Heterocyclizations of Functionalized Heterocumulenes with C,N- and C,O-Dinucleophiles: III.* Cyclization of N-(1-Aryl-1-chloro-2,2,2-trifluoroethyl)-N'-arylcarbodiimides with 3-Substituted 1-Phenylpyrazol-5-ones. Russian Journal of Organic Chemistry. 39(12). 1789–1791.

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