V. D. Dyachenko

1.9k total citations
223 papers, 1.2k citations indexed

About

V. D. Dyachenko is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, V. D. Dyachenko has authored 223 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 217 papers in Organic Chemistry, 22 papers in Molecular Biology and 22 papers in Pharmacology. Recurrent topics in V. D. Dyachenko's work include Synthesis of heterocyclic compounds (113 papers), Synthesis and Characterization of Heterocyclic Compounds (111 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (94 papers). V. D. Dyachenko is often cited by papers focused on Synthesis of heterocyclic compounds (113 papers), Synthesis and Characterization of Heterocyclic Compounds (111 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (94 papers). V. D. Dyachenko collaborates with scholars based in Ukraine, Russia and Mozambique. V. D. Dyachenko's co-authors include В. П. Литвинов, I. V. Dyachenko, С. Г. Кривоколыско, Valentine G. Nenajdenko, Alexander N. Chernega, Эдуард Б. Русанов, Victor N. Khrustalev, Павел В. Дороватовский, В. П. Литвинов and Vladimir N. Nesterov and has published in prestigious journals such as Synlett, Russian Chemical Reviews and Russian Chemical Bulletin.

In The Last Decade

V. D. Dyachenko

205 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. D. Dyachenko Ukraine 14 1.2k 151 124 112 26 223 1.2k
Hanafi H. Zoorob Egypt 20 954 0.8× 164 1.1× 75 0.6× 189 1.7× 35 1.3× 90 1.1k
А. М. Шестопалов Russia 17 1.2k 1.0× 124 0.8× 278 2.2× 63 0.6× 19 0.7× 101 1.2k
Hideki Jona Japan 16 649 0.6× 490 3.2× 107 0.9× 63 0.6× 31 1.2× 36 761
Kei Kitamura Japan 10 519 0.4× 183 1.2× 102 0.8× 38 0.3× 31 1.2× 29 575
Sabita Nayak India 19 913 0.8× 174 1.2× 129 1.0× 83 0.7× 67 2.6× 73 1.0k
Marwa A.M.Sh. El‐Sharief Egypt 16 668 0.6× 195 1.3× 70 0.6× 52 0.5× 22 0.8× 27 773
M. HOSHINO Japan 12 533 0.5× 224 1.5× 68 0.5× 41 0.4× 49 1.9× 21 648
Birsen Tozkoparan Türkiye 15 1.1k 0.9× 202 1.3× 122 1.0× 27 0.2× 29 1.1× 52 1.2k
Christopher C. Nawrat United Kingdom 14 662 0.6× 171 1.1× 78 0.6× 75 0.7× 52 2.0× 26 821
V. A. Osyanin Russia 15 867 0.8× 105 0.7× 227 1.8× 118 1.1× 12 0.5× 127 935

Countries citing papers authored by V. D. Dyachenko

Since Specialization
Citations

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

Fields of papers citing papers by V. D. Dyachenko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. D. Dyachenko

This figure shows the co-authorship network connecting the top 25 collaborators of V. D. Dyachenko. A scholar is included among the top collaborators of V. D. Dyachenko 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. D. Dyachenko. V. D. Dyachenko 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.
Dyachenko, V. D., et al.. (2025). Optical Absorption Spectra of (E)-2-(2-Aryl-1-Cyanovinyl)-4-Cyclopropylthiazoles. Journal of Applied Spectroscopy. 92(1). 16–25.
2.
Dyachenko, I. V., et al.. (2024). Cyanothioacetamide in Multicomponent Synthesis of 2-Thionicotinonitrile Derivatives. Russian Journal of General Chemistry. 94(6). 1217–1230.
3.
Dyachenko, I. V., V. D. Dyachenko, Павел В. Дороватовский, Victor N. Khrustalev, & Valentine G. Nenajdenko. (2024). Multicomponent Synthesis of Nicotinamide and Thieno[2,3-b]pyridine Derivatives. Russian Journal of Organic Chemistry. 60(4). 588–600. 1 indexed citations
4.
Dyachenko, I. V., V. D. Dyachenko, Павел В. Дороватовский, Victor N. Khrustalev, & Valentine G. Nenajdenko. (2023). Multicomponent synthesis of functionalized 2-amino-4<i>H</i>-pyrans initiated by the Knoevenagel reaction. Журнал органической химии. 59(2). 197–210. 1 indexed citations
5.
Dyachenko, I. V., et al.. (2023). New Syntheses of Cycloalka[c]pyridine-3-carboxamide and -carbonitrile Derivatives. Russian Journal of Organic Chemistry. 59(6). 969–979. 2 indexed citations
6.
Dyachenko, I. V., V. D. Dyachenko, Павел В. Дороватовский, Victor N. Khrustalev, & Valentine G. Nenajdenko. (2023). Multicomponent Synthesis of Pyridine and Pyrimidine Derivatives Initiated by the Knoevenagel Reaction. Russian Journal of General Chemistry. 93(S1). S61–S72. 1 indexed citations
7.
Dyachenko, I. V., V. D. Dyachenko, Павел В. Дороватовский, et al.. (2022). Three-Component Synthesis and Crystal Structure of 2-Amino-3-cyano-4H-pyran and -thiopyran Derivatives. Russian Journal of Organic Chemistry. 58(12). 1786–1796. 1 indexed citations
8.
Dyachenko, I. V., V. D. Dyachenko, Павел В. Дороватовский, Victor N. Khrustalev, & Valentine G. Nenajdenko. (2022). Selectivity of Alkylation of Malononitrile Derivatives with α-Bromocarbonyl Compounds. Russian Journal of Organic Chemistry. 58(12). 1769–1779. 1 indexed citations
9.
Dyachenko, I. V., et al.. (2018). A New Version of Multicomponent Synthesis of 4,6-Diaryl-2-sulfanylidene-1,2-dihydropyridine-3-carbonitrile Derivatives. Russian Journal of Organic Chemistry. 54(9). 1273–1284. 3 indexed citations
10.
Dyachenko, I. V., V. D. Dyachenko, Павел В. Дороватовский, Victor N. Khrustalev, & Valentine G. Nenajdenko. (2018). Multicomponent Synthesis of 4-Alkyl(Aryl, Hetaryl)-2-alkoxycarbonyl(aroyl, carbamoyl)- 3,6-diamino-5-cyanothieno[2,3-b]pyridines. Russian Journal of Organic Chemistry. 54(10). 1435–1445. 8 indexed citations
11.
Dyachenko, V. D., et al.. (2013). Recyclization of 4-alkyl(aryl)-2,6-diamino-3,5-dicyano-4H-thiopyrans with 2-aminoethanol and (2-furyl)methylamine. Chemistry of Heterocyclic Compounds. 49(6). 897–901. 1 indexed citations
12.
13.
Dyachenko, V. D., et al.. (2010). Synthesis of new 2-thioxo-1,2,3,4-tetrahydropyridine-3-carboxanilides and their alkylation. Russian Journal of General Chemistry. 80(2). 330–333. 4 indexed citations
14.
15.
Dyachenko, V. D.. (2005). Isovaleric Aldehyde in the Synthesis of 4-Isobutyl-Substituted Pyridine-2(1H)-thiones, 4H-Pyrans, and 1,3-Cyclohexadiene. Russian Journal of General Chemistry. 75(3). 440–446. 12 indexed citations
16.
17.
Кривоколыско, С. Г., V. D. Dyachenko, & В. П. Литвинов. (2000). A convenient method for the synthesis of substituted 2-alkylthio-3-cyano-4,6-dimethyl-5-phenylcarbamoyl-1,4-dihydropyridines. Chemistry of Heterocyclic Compounds. 36(3). 284–286. 2 indexed citations
18.
Кривоколыско, С. Г., V. D. Dyachenko, & В. П. Литвинов. (1999). Thienylmethylenecyanothioacetamide and 2-acetoacetotoluidine in the synthesis of substituted di-and tetrahydro-3-cyanopyridine-2-thiolates. Chemistry of Heterocyclic Compounds. 35(10). 1190–1195. 2 indexed citations
19.
Кривоколыско, С. Г., V. D. Dyachenko, & В. П. Литвинов. (1999). Aliphatic aldehydes in synthesis of 4-alkyl-5-carbamoyl-3-cyano-6-methylpyridine-2(1H)-thiones. Chemistry of Heterocyclic Compounds. 35(2). 204–205.
20.
Nesterov, Vladimir N., Valery Shklover, Yu. T. Struchkov, Yu. A. Sharanin, & V. D. Dyachenko. (1989). Synthesis and properties of 4,6-diamino-3-cyano-2(1H)-pyridineselenone: Molecular and crystal structure of 2-allylseleno-4,6-diamino-3-cyanopyridine. Russian Chemical Bulletin. 38(11). 2372–2376. 1 indexed citations

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