О. Е. Насакин

1.3k total citations
197 papers, 998 citations indexed

About

О. Е. Насакин is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, О. Е. Насакин has authored 197 papers receiving a total of 998 indexed citations (citations by other indexed papers that have themselves been cited), including 172 papers in Organic Chemistry, 24 papers in Molecular Biology and 10 papers in Spectroscopy. Recurrent topics in О. Е. Насакин's work include Synthesis and Reactions of Organic Compounds (44 papers), Synthesis and Reactivity of Heterocycles (43 papers) and Synthesis of heterocyclic compounds (43 papers). О. Е. Насакин is often cited by papers focused on Synthesis and Reactions of Organic Compounds (44 papers), Synthesis and Reactivity of Heterocycles (43 papers) and Synthesis of heterocyclic compounds (43 papers). О. Е. Насакин collaborates with scholars based in Russia, Tajikistan and Zimbabwe. О. Е. Насакин's co-authors include О. В. Ершов, В. А. Тафеенко, Ya. S. Kayukov, И. Н. Бардасов, М. Yu. Belikov, Mikhail Yu. Ievlev, Anastasiya U. Alekseeva, Sergey V. Fedoseev, В. Л. Гейн and Evgeniya V. Nurieva and has published in prestigious journals such as International Journal of Molecular Sciences, Green Chemistry and The Journal of Organic Chemistry.

In The Last Decade

О. Е. Насакин

166 papers receiving 993 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
О. Е. Насакин Russia 16 909 129 108 65 61 197 998
Toshiyuki Hamura Japan 19 915 1.0× 80 0.6× 66 0.6× 54 0.8× 22 0.4× 56 984
Wilhelm Flitsch Germany 16 769 0.8× 116 0.9× 155 1.4× 33 0.5× 48 0.8× 106 874
И. Б. Розенцвейг Russia 13 600 0.7× 70 0.5× 149 1.4× 15 0.2× 75 1.2× 150 737
Komal Aggarwal India 12 220 0.2× 106 0.8× 77 0.7× 41 0.6× 118 1.9× 22 378
Áron Pintér Germany 16 625 0.7× 79 0.6× 111 1.0× 16 0.2× 89 1.5× 20 750
Wolfgang Eberbach Germany 19 1.1k 1.2× 89 0.7× 141 1.3× 27 0.4× 33 0.5× 90 1.1k
L. FISERA Slovakia 15 963 1.1× 35 0.3× 239 2.2× 45 0.7× 33 0.5× 119 1.0k
А. Н. Масливец Russia 14 1.4k 1.6× 20 0.2× 108 1.0× 52 0.8× 32 0.5× 331 1.5k
Masahiro Ariga Japan 18 905 1.0× 61 0.5× 246 2.3× 19 0.3× 36 0.6× 96 971
I. CSOEREGH Sweden 12 392 0.4× 66 0.5× 179 1.7× 18 0.3× 61 1.0× 16 561

Countries citing papers authored by О. Е. Насакин

Since Specialization
Citations

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

Fields of papers citing papers by О. Е. Насакин

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by О. Е. Насакин. 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 О. Е. Насакин. The network helps show where О. Е. Насакин may publish in the future.

Co-authorship network of co-authors of О. Е. Насакин

This figure shows the co-authorship network connecting the top 25 collaborators of О. Е. Насакин. A scholar is included among the top collaborators of О. Е. Насакин 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 О. Е. Насакин. О. Е. Насакин 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.
Fedoseev, Sergey V., et al.. (2024). Tunable full-color dual-state (solution and solid) emission of push–pull molecules containing the 1-pyrindane moiety. Beilstein Journal of Organic Chemistry. 20. 3016–3025. 2 indexed citations
2.
Насакин, О. Е., et al.. (2024). Synthesis and Photophysical Properties of Ethyl 3,6-Diamino-4-aryl-5-cyanothieno[2,3-b]pyridine-2-carboxylates. Russian Journal of General Chemistry. 94(8). 1930–1934. 1 indexed citations
3.
Насакин, О. Е., et al.. (2023). Implementation of Zincke reaction in one-pot synthesis of switchable, Ag+ and Hg2+ sensing aza-merocyanines based on α-aminopyridin-3,5-dicarbonitrile moiety. Tetrahedron Letters. 125. 154625–154625. 2 indexed citations
4.
Насакин, О. Е., et al.. (2023). One-pot transformations of tetracyanocyclopropanes into highly functionalized pyridines. Chemistry of Heterocyclic Compounds. 59(8). 610–613. 3 indexed citations
5.
Насакин, О. Е., et al.. (2023). Voltammetric Determination of Diphenhydramine Hydrochloride in Solid and Liquid Dosage Forms. Pharmaceutical Chemistry Journal. 56(12). 1671–1676.
6.
Belikov, М. Yu., et al.. (2020). Novel approach to the synthesis and optical absorption properties of 2-(2-oxo-1,2-dihydro-3 H- pyrrole-3-ylidene)malononitriles. Synthetic Communications. 51(5). 727–737. 5 indexed citations
7.
Насакин, О. Е., et al.. (2020). Application of Photogenerated Iodine for Quantitative Determination of Water-Soluble Antioxidants. Pharmaceutical Chemistry Journal. 54(8). 851–856.
8.
Shtyrlin, Nikita V., et al.. (2018). Synthesis, antibacterial and antitumor activity of methylpyridinium salts of pyridoxine functionalized 2-amino-6-sulfanylpyridine-3,5-dicarbonitriles. Synthetic Communications. 48(17). 2288–2304. 17 indexed citations
9.
Ievlev, Mikhail Yu., et al.. (2016). Diastereoselective synthesis of 3,4-dihydro-2H-pyran-4-carboxamides through an unusual regiospecific quasi-hydrolysis of a cyano group. Beilstein Journal of Organic Chemistry. 12. 2093–2098. 10 indexed citations
10.
11.
Ершов, О. В., et al.. (2012). Synthesis and reactivity of methyl 3-acyl-6-amino-4-aryl-5-cyano-4H-pyran-2-carboxylates. Chemistry of Heterocyclic Compounds. 48(7). 997–1005. 1 indexed citations
12.
Belikov, М. Yu., et al.. (2010). Synthesis of a new organic anion by reaction of 4-aryl(hetaryl)-4-oxobutane-1,1,2,2-tetracarbonitriles with ammonia. Russian Journal of Organic Chemistry. 46(4). 597–598. 7 indexed citations
13.
Kayukov, Ya. S., et al.. (2004). Synthesis of 6,6-dialkyl-4,8-dioxo-5,7-dioxaspiro[2.5]octane-1,1,2,2- tetracarbonitriles and 2,2,3,3-tetracyanocyclopropanecarboxylic acid. Russian Journal of Organic Chemistry. 40(9). 1382–1383. 5 indexed citations
14.
Ершов, О. В., et al.. (2002). Decyanation of 5-Alkyl-6-aryl-4-oxocyclohexane-1,1,2,2-tetracarbonitriles. Russian Journal of Organic Chemistry. 38(7). 1068–1069.
15.
Ершов, О. В., et al.. (2000). A new route to 1-substituted 2,2,3,3-tetracyanocyclopropanes. Russian Journal of General Chemistry. 70(8). 1251–1253. 2 indexed citations
16.
Ершов, О. В., et al.. (2000). Reaction of tetracyanoethylene with alpha,beta-unsaturated ketones. Russian Journal of Organic Chemistry. 36(4). 593–594. 1 indexed citations
17.
Насакин, О. Е., et al.. (1998). Synthesis of 2,6-disubstituted 3,3,5,5-tetracyanopiperidines by the reaction of 1,1,3,3-tetracyanopropane with 2,4-diazapentane-1,4-dienes. Chemistry of Heterocyclic Compounds. 34(10). 1177–1180.
18.
Насакин, О. Е., et al.. (1991). Cyclization of 1,1,2,2-tetracyanoethane by the semicarbazones and oximes of carbonyl compounds. Chemistry of Heterocyclic Compounds. 27(8). 837–841.
19.
Насакин, О. Е., et al.. (1984). ジチオりん酸O,O‐ジアルキルとテトラシアノアルカノンとの反応. 54(2). 470–471. 2 indexed citations
20.
Насакин, О. Е., et al.. (1984). Reaction of tetracyanoethylated ketones with aldehydes. Synthesis of 3-imino-2,6-dioxabicyclo[2.2.2]octanes. Chemistry of Heterocyclic Compounds. 20(11). 1206–1210. 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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