З. В. Степанова

486 total citations
33 papers, 383 citations indexed

About

З. В. Степанова is a scholar working on Organic Chemistry, Materials Chemistry and Physical and Theoretical Chemistry. According to data from OpenAlex, З. В. Степанова has authored 33 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Organic Chemistry, 11 papers in Materials Chemistry and 7 papers in Physical and Theoretical Chemistry. Recurrent topics in З. В. Степанова's work include Synthesis and Characterization of Pyrroles (21 papers), Porphyrin and Phthalocyanine Chemistry (11 papers) and Fluorine in Organic Chemistry (6 papers). З. В. Степанова is often cited by papers focused on Synthesis and Characterization of Pyrroles (21 papers), Porphyrin and Phthalocyanine Chemistry (11 papers) and Fluorine in Organic Chemistry (6 papers). З. В. Степанова collaborates with scholars based in Russia, Canada and China. З. В. Степанова's co-authors include Б. А. Трофимов, Lyubov N. Sobenina, А. Й. Михалева, Igor А. Ushakov, О. В. Петрова, T. I. Vakul’skaya, О.Н. Кажева, А. В. Афонин, O.A. Dyachenko and В. Н. Елохина and has published in prestigious journals such as Tetrahedron, Tetrahedron Letters and Synthesis.

In The Last Decade

З. В. Степанова

32 papers receiving 366 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
З. В. Степанова Russia 11 334 100 62 50 45 33 383
J. A. VAN ALLAN United States 9 278 0.8× 98 1.0× 52 0.8× 36 0.7× 39 0.9× 38 358
Tetsuro Shimo Japan 13 420 1.3× 63 0.6× 55 0.9× 78 1.6× 14 0.3× 64 474
Г. А. Душенко Russia 13 378 1.1× 159 1.6× 77 1.2× 18 0.4× 73 1.6× 84 509
Kazuhiro Yoshizawa Japan 11 219 0.7× 44 0.4× 49 0.8× 20 0.4× 38 0.8× 22 281
Валентина А. Карноухова Russia 11 220 0.7× 90 0.9× 76 1.2× 26 0.5× 28 0.6× 42 346
Alexander V. Mazepa Ukraine 11 270 0.8× 37 0.4× 86 1.4× 19 0.4× 32 0.7× 48 340
I. V. BODRIKOV Russia 9 271 0.8× 31 0.3× 33 0.5× 40 0.8× 67 1.5× 52 375
Piero Sarti‐Fantoni Italy 12 382 1.1× 79 0.8× 60 1.0× 59 1.2× 39 0.9× 41 482
Rajive K. Khanna India 11 232 0.7× 47 0.5× 46 0.7× 17 0.3× 17 0.4× 21 311
Ilya N. Egorov Russia 8 286 0.9× 47 0.5× 36 0.6× 24 0.5× 21 0.5× 32 356

Countries citing papers authored by З. В. Степанова

Since Specialization
Citations

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

Fields of papers citing papers by З. В. Степанова

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of З. В. Степанова

This figure shows the co-authorship network connecting the top 25 collaborators of З. В. Степанова. A scholar is included among the top collaborators of З. В. Степанова 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 З. В. Степанова. З. В. Степанова 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.
Sobenina, Lyubov N., З. В. Степанова, Igor А. Ushakov, et al.. (2011). From 4,5,6,7-tetrahydroindole to functionalized furan-2-one–4,5,6,7-tetrahydroindole–cyclobutene sequence in two steps. Tetrahedron. 67(26). 4832–4837. 12 indexed citations
2.
Трофимов, Б. А., Lyubov N. Sobenina, З. В. Степанова, et al.. (2010). Rearrangements of the [2+2]-cycloadducts of DDQ and 2-ethynylpyrroles. Tetrahedron Letters. 51(38). 5028–5031. 13 indexed citations
3.
Трофимов, Б. А., Lyubov N. Sobenina, З. В. Степанова, et al.. (2008). Chemo- and regioselective ethynylation of 4,5,6,7-tetrahydroindoles with ethyl 3-halo-2-propynoates. Tetrahedron Letters. 49(24). 3946–3949. 17 indexed citations
4.
Трофимов, Б. А., Lyubov N. Sobenina, A. P. Demenev, et al.. (2007). A palladium- and copper-free cross-coupling of ethyl 3-halo-2-propynoates with 4,5,6,7-tetrahydroindoles on alumina. Tetrahedron Letters. 48(27). 4661–4664. 17 indexed citations
5.
Трофимов, Б. А., Lyubov N. Sobenina, З. В. Степанова, et al.. (2007). Synthesis of 2‐Benzoylethynylpyrroles by Cross Coupling of 2‐Arylpyrroles with 1‐Benzoyl‐2‐bromoacetylene over Aluminum Oxide.. ChemInform. 38(9). 1 indexed citations
6.
Трофимов, Б. А., Lyubov N. Sobenina, З. В. Степанова, et al.. (2006). Synthesis of 2-benzoylethynylpyrroles by cross coupling of 2-arylpyrroles with 1-benzoyl-2-bromoacetylene over aluminum oxide. Russian Journal of Organic Chemistry. 42(9). 1348–1355. 10 indexed citations
7.
Афонин, А. В., Igor А. Ushakov, Lyubov N. Sobenina, et al.. (2005). Different types of hydrogen bonds in 2‐substituted pyrroles and 1‐vinyl pyrroles as monitored by 1H, 13C and 15N NMR spectroscopy and ab initio calculations. Magnetic Resonance in Chemistry. 44(1). 59–65. 33 indexed citations
8.
Степанова, З. В., А. Й. Михалева, Igor А. Ushakov, et al.. (2004). Silica-Assisted Reactions of Pyrroles with 1-Acyl-2-bromoacetylenes. Synthesis. 2004(16). 2736–2742. 4 indexed citations
9.
Трофимов, Б. А., З. В. Степанова, Lyubov N. Sobenina, А. Й. Михалева, & Igor А. Ushakov. (2004). Ethynylation of pyrroles with 1-acyl-2-bromoacetylenes on alumina: a formal ‘inverse Sonogashira coupling’. Tetrahedron Letters. 45(34). 6513–6516. 92 indexed citations
10.
Степанова, З. В., Lyubov N. Sobenina, А. Й. Михалева, et al.. (2003). Synthesis and X-Ray Diffraction Study of 2-(2-Acyl-1-phenylethenyl)pyrroles. Russian Journal of Organic Chemistry. 39(11). 1636–1643. 6 indexed citations
11.
Ushakov, Igor А., А. В. Афонин, В. К. Воронов, et al.. (2003). NMR Study of the Steric and Electronic Structure of 2-(2-Acylethenyl)pyrroles. Russian Journal of Organic Chemistry. 39(9). 1318–1324. 11 indexed citations
12.
Ushakov, Igor А., А. В. Афонин, В. К. Воронов, et al.. (2002). 1H and 13C NMR Study of Steric and Electronic Structure of 2-(2-Acylethenyl)-1-vinylpyrroles. Russian Journal of Organic Chemistry. 38(12). 1775–1781. 3 indexed citations
13.
Sobenina, Lyubov N., A. P. Demenev, А. Й. Михалева, et al.. (2001). Reactions of Pyrrole-1- and Pyrrole-2-carbodithioates with Activated Acetylenes. Russian Journal of Organic Chemistry. 37(4). 547–551. 3 indexed citations
14.
Трофимов, Б. А., З. В. Степанова, Lyubov N. Sobenina, et al.. (2001). C-Vinylation of 1-Vinylpyrroles with Benzoylacetylene on Silica Gel. Synthesis. 2001(12). 1878–1882. 4 indexed citations
15.
Chípanina, N. N., et al.. (2000). Synthesis and IR spectra of 5-phenyl-2-(1-phenyl-2-trichloroacetylethenyl)pyrrole. Russian Chemical Bulletin. 49(11). 1914–1916. 8 indexed citations
16.
Трофимов, Б. А., З. В. Степанова, Lyubov N. Sobenina, et al.. (1999). Pyrroles as C-nucleophiles in reactions with acylacetylenes. Russian Chemical Bulletin. 48(8). 1542–1547. 8 indexed citations
17.
Трофимов, Б. А., et al.. (1999). Reaction of 2-phenylpyrrole with 2-acyl-1-phenylacetylenes on silicon dioxide. Chemistry of Heterocyclic Compounds. 35(9). 1107–1108. 3 indexed citations
18.
Трофимов, Б. А., З. В. Степанова, Igor А. Ushakov, et al.. (1998). An example of the facile C-vinylation of pyrroles. Mendeleev Communications. 8(3). 119–119. 9 indexed citations
19.
Воронков, М. Г., З. В. Степанова, А. В. Афонин, & В. К. Воронов. (1987). Synthesis and structure of 1,3-divinyl-5-halouracils. Russian Chemical Bulletin. 36(3). 614–616. 1 indexed citations
20.
Andriyankova, Ludmila V., et al.. (1983). Reaction of salicylic acid derivatives with acetylene. Russian Chemical Bulletin. 32(10). 2153–2155. 1 indexed citations

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