С. В. Амосова

3.6k total citations
336 papers, 2.6k citations indexed

About

С. В. Амосова is a scholar working on Organic Chemistry, Toxicology and Inorganic Chemistry. According to data from OpenAlex, С. В. Амосова has authored 336 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 286 papers in Organic Chemistry, 214 papers in Toxicology and 38 papers in Inorganic Chemistry. Recurrent topics in С. В. Амосова's work include Organoselenium and organotellurium chemistry (214 papers), Sulfur-Based Synthesis Techniques (93 papers) and Organic Chemistry Cycloaddition Reactions (83 papers). С. В. Амосова is often cited by papers focused on Organoselenium and organotellurium chemistry (214 papers), Sulfur-Based Synthesis Techniques (93 papers) and Organic Chemistry Cycloaddition Reactions (83 papers). С. В. Амосова collaborates with scholars based in Russia, India and United States. С. В. Амосова's co-authors include В. А. Потапов, М. В. Мусалов, М. В. Пензик, М. В. Мусалова, Alexander I. Albanov, А. В. Мартынов, Б. А. Трофимов, Barry R. Steele, Ioannis D. Kostas and Yury Yu. Rusakov and has published in prestigious journals such as International Journal of Molecular Sciences, Physical Chemistry Chemical Physics and The Journal of Organic Chemistry.

In The Last Decade

С. В. Амосова

305 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
С. В. Амосова Russia	25	2.3k	1.8k	350	221	130	336	2.6k
Luana Bagnoli Italy	29	2.1k 0.9×	1.2k 0.7×	380 1.1×	126 0.6×	274 2.1×	106	2.4k
Sangit Kumar India	34	3.0k 1.3×	1.4k 0.8×	444 1.3×	88 0.4×	231 1.8×	98	3.4k
A. Panda India	17	966 0.4×	798 0.4×	376 1.1×	128 0.6×	71 0.5×	24	1.4k
Alexander I. Albanov Russia	18	1.4k 0.6×	425 0.2×	310 0.9×	114 0.5×	138 1.1×	248	1.6k
Andrea Temperini Italy	28	1.8k 0.8×	854 0.5×	317 0.9×	126 0.6×	358 2.8×	108	2.1k
Sergey Belyakov Latvia	21	1.2k 0.5×	256 0.1×	350 1.0×	133 0.6×	271 2.1×	233	1.8k
Pavel Arsenyan Latvia	21	931 0.4×	542 0.3×	131 0.4×	83 0.4×	208 1.6×	135	1.4k
Claude Paulmier France	16	993 0.4×	642 0.4×	123 0.4×	156 0.7×	159 1.2×	50	1.3k
Bani Kanta Sarma India	15	717 0.3×	632 0.4×	111 0.3×	78 0.4×	335 2.6×	31	1.2k
M. Renson Belgium	21	982 0.4×	661 0.4×	175 0.5×	202 0.9×	83 0.6×	117	1.3k

Countries citing papers authored by С. В. Амосова

Since Specialization

Citations

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

Fields of papers citing papers by С. В. Амосова

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of С. В. Амосова

This figure shows the co-authorship network connecting the top 25 collaborators of С. В. Амосова. A scholar is included among the top collaborators of С. В. Амосова 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 С. В. Амосова. С. В. Амосова 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

Амосова, С. В., et al.. (2023). Efficient Regioselective Synthesis of Novel Ensembles of Organylselanyl-Functionalized Divinyl Sulfides and 1,3-Thiaselenoles under Phase Transfer Catalysis Conditions. Catalysts. 13(8). 1227–1227. 1 indexed citations

Амосова, С. В., et al.. (2023). Green Organoselenium Chemistry: Selective Syntheses of New 1,4-Thiaselenine Derivatives Based on Reactions of Thiaselenole Reagent with Alcohols and Water. Inorganics. 11(7). 281–281. 1 indexed citations

Потапов, В. А., et al.. (2022). Regio- and Stereoselective Synthesis of (Z,Z)-Bis(3-amino-3-oxo-1-propenyl) Selenides and Diselenides Based on 2-propynamides: A Novel Family of Diselenides with High Glutathione Peroxidase-like Activity. Inorganics. 10(6). 74–74. 3 indexed citations

Ogienko, Andrey G., Andrey G. Ogienko, S. A. Myz, et al.. (2022). Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon. Pharmaceutics. 14(3). 495–495. 4 indexed citations

Мусалов, М. В., et al.. (2021). A Regioselective Synthesis of Novel Functionalized Organochalcogen Compounds by Chalcogenocyclofunctionalization Reactions Based on Chalcogen Halides and Natural Products. Molecules. 26(12). 3729–3729. 5 indexed citations

Потапов, В. А., et al.. (2020). (Z,Z)-Selanediylbis(2-propenamides): Novel Class of Organoselenium Compounds with High Glutathione Peroxidase-Like Activity. Regio- and Stereoselective Reaction of Sodium Selenide with 3-Trimethylsilyl-2-propynamides. Molecules. 25(24). 5940–5940. 6 indexed citations

Потапов, В. А., et al.. (2018). Bis(tetrahydro-2H-pyran-2-ylmethyl)sulfide and -Sulfoxide from Sulfur Dichloride and 5-Hexen-1-ol. Russian Journal of General Chemistry. 88(12). 2689–2690.

Потапов, В. А., et al.. (2018). Regio- and Stereoselective Synthesis of Functionalized Vinyl Sulfides Based on Pyridine-2-thiol and Propynoic Acid and Its Derivatives. Russian Journal of Organic Chemistry. 54(12). 1798–1802. 2 indexed citations

Мартынов, А. В., et al.. (2016). Synthesis of new heterocycles by oxidation of functionalized cyclic derivatives of bis(2-chlorovinyl) sulfide and selenide. Russian Journal of Organic Chemistry. 52(6). 887–891. 3 indexed citations

10.

Мусалов, М. В., В. А. Потапов, М. В. Мусалова, & С. В. Амосова. (2015). First synthesis of hept-6-en-1,3-diyne. Russian Chemical Bulletin. 64(9). 2273–2274. 1 indexed citations

11.

Пензик, М. В., С. В. Амосова, А. И. Албанов, & В. А. Потапов. (2014). Unexpected regio- and stereoselective reaction of 2-bromomethyl-1,3-thiaselenole with ketones. Formation of 1-[(Z)-2-(vinylsulfanyl)ethenyl]selanylalkan-2-ones. Russian Journal of Organic Chemistry. 50(6). 916–918. 4 indexed citations

12.

Амосова, С. В., М. В. Пензик, В. А. Потапов, & A. I. Albanov. (2013). Synthesis of 2,6-dichloro-1,4-dithiane. The effect of the chalcogen nature on the stability of 2,6-dichloro-1,4-thiachalcogenanes. Chemistry of Heterocyclic Compounds. 48(11). 1716–1718. 3 indexed citations

13.

Rusakov, Yury Yu., Leonid B. Krivdin, В. А. Потапов, М. В. Пензик, & С. В. Амосова. (2011). Conformational analysis and diastereotopic assignments in the series of selenium‐containing heterocycles by means of ⁷⁷Se‐¹H spin‐spin coupling constants: a combined theoretical and experimental study. Magnetic Resonance in Chemistry. 49(7). 389–398. 35 indexed citations

14.

Амосова, С. В., et al.. (2010). New Methodology of Heterocyclization: the Electrophilic Addition Reactions of Selenium Di- and Tetrahalides and Tellurium Tetrachloride to Diethynyl Silanes and Germanes. Mini-Reviews in Organic Chemistry. 7(1). 23–32. 10 indexed citations

15.

Амосова, С. В., М. В. Пензик, В. А. Потапов, & А. И. Албанов. (2008). A reaction of selenium dichloride with divinyl sulfide. Russian Chemical Bulletin. 57(6). 1323–1323. 7 indexed citations

16.

Амосова, С. В., et al.. (2003). Divinyl Sulfide as Synthetic Equivalent of Ethenethiolate and 3-Butenethiolate Anions in Nucleophilic Substitution in Halopyridines and Haloalkanes. Russian Journal of Organic Chemistry. 39(5). 713–717. 4 indexed citations

17.

Амосова, С. В., et al.. (1994). Synthesis and biological activity of 1-organylsulfinyl-3-allylsulfinyl-1-propenes. Pharmaceutical Chemistry Journal. 28(1). 36–39.

18.

Амосова, С. В., et al.. (1988). Preparative synthesis of divinyl ditelluride. 24(2). 454–455. 1 indexed citations

19.

Потапов, В. А., et al.. (1988). Divinylethylselenonium tetrafluoroborate ? A reactive monomer and first example of a vinylselenonium compound. Russian Chemical Bulletin. 37(4). 823–823. 1 indexed citations

20.

Трофимов, Б.А., et al.. (1985). New method of synthesis of alkylvinyltellurides. 21(5). 1130–1131.

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