А. Й. Михалева

3.9k total citations
320 papers, 3.0k citations indexed

About

А. Й. Михалева is a scholar working on Organic Chemistry, Materials Chemistry and Pharmaceutical Science. According to data from OpenAlex, А. Й. Михалева has authored 320 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 270 papers in Organic Chemistry, 125 papers in Materials Chemistry and 101 papers in Pharmaceutical Science. Recurrent topics in А. Й. Михалева's work include Synthesis and Characterization of Pyrroles (161 papers), Porphyrin and Phthalocyanine Chemistry (113 papers) and Fluorine in Organic Chemistry (100 papers). А. Й. Михалева is often cited by papers focused on Synthesis and Characterization of Pyrroles (161 papers), Porphyrin and Phthalocyanine Chemistry (113 papers) and Fluorine in Organic Chemistry (100 papers). А. Й. Михалева collaborates with scholars based in Russia, France and China. А. Й. Михалева's co-authors include Б. А. Трофимов, Igor А. Ushakov, Lyubov N. Sobenina, Elena Yu. Schmidt, А. М. Васильцов, Nadezhda V. Zorina, О. В. Петрова, A. P. Demenev, Alexey B. Zaitsev and А. В. Иванов and has published in prestigious journals such as Chemical Reviews, Chemical Communications and Electrochimica Acta.

In The Last Decade

А. Й. Михалева

297 papers receiving 2.9k citations

Peers

А. Й. Михалева
Ung Chan Yoon South Korea
Kazuhiko Mizuno Japan
L. Malpezzi Italy
Kazumasa Funabiki Japan
Igor А. Ushakov Russia
L. R. Subramanian Germany
Valerian T. D’Souza United States
Shuntarō Mataka Japan
Frédéric Hapiot France
Yaofeng Yuan China
Ung Chan Yoon South Korea
А. Й. Михалева
Citations per year, relative to А. Й. Михалева А. Й. Михалева (= 1×) peers Ung Chan Yoon

Countries citing papers authored by А. Й. Михалева

Since Specialization
Citations

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

Fields of papers citing papers by А. Й. Михалева

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by А. Й. Михалева. 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 А. Й. Михалева. The network helps show where А. Й. Михалева may publish in the future.

Co-authorship network of co-authors of А. Й. Михалева

This figure shows the co-authorship network connecting the top 25 collaborators of А. Й. Михалева. A scholar is included among the top collaborators of А. Й. Михалева 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 А. Й. Михалева. А. Й. Михалева 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.
2.
Михалева, А. Й., О. В. Петрова, & Lyubov N. Sobenina. (2013). 2-PHENYLPYRROLE: ONE-POT SELECTIVE SYNTHESIS FROM ACETOPHENONE OXIME AND ACETYLENE BY A TROFIMOV REACTION. Chemistry of Heterocyclic Compounds. 1649–1653. 6 indexed citations
3.
Protsuk, Nadezhda I., et al.. (2013). Improved method for the synthesis of 1-vinylindole. Chemistry of Heterocyclic Compounds. 49(3). 404–407. 13 indexed citations
4.
Трофимов, Б. А., А. В. Иванов, Igor А. Ushakov, et al.. (2012). Metallation of N-vinylpyrroles and -indoles with Hg(OAc)2: N-vinyl vs. pyrrole nucleophilic sites. Dalton Transactions. 41(18). 5512–5512. 6 indexed citations
5.
Schmidt, Elena Yu., Nadezhda V. Zorina, Marina Yu. Dvorko, et al.. (2011). A General Synthetic Strategy for the Design of New BODIPY Fluorophores Based on Pyrroles with Polycondensed Aromatic and Metallocene Substituents. Chemistry - A European Journal. 17(11). 3069–3073. 32 indexed citations
6.
Zhang, Kai, Fangbin Gong, Shayu Li, et al.. (2011). A new fluorescent chemosensor for fluoride anion based on a pyrrole–isoxazole derivative. Beilstein Journal of Organic Chemistry. 7. 46–52. 49 indexed citations
7.
Трофимов, Б. А., А. Й. Михалева, А. М. Васильцов, et al.. (2010). Selective dehydrogenation of 4,5,6,7-tetrahydroindole to indole with a nickel sulfide catalyst. Doklady Chemistry. 434(2). 257–259. 2 indexed citations
8.
Трофимов, Б. А., Elena Yu. Schmidt, Igor А. Ushakov, et al.. (2010). Base‐Catalyzed Stereoselective Vinylation of Ketones with Arylacetylenes: A New C(sp3)C(sp2) Bond‐Forming Reaction. Chemistry - A European Journal. 16(28). 8516–8521. 70 indexed citations
9.
10.
Трофимов, Б. А., Elena Yu. Schmidt, А. Й. Михалева, et al.. (2009). Synthesis of 2‐(Selenophen‐2‐yl)pyrroles and Their Electropolymerization to Electrochromic Nanofilms. Chemistry - A European Journal. 15(26). 6435–6445. 18 indexed citations
11.
Schmidt, Elena Yu., Б. А. Трофимов, А. Й. Михалева, et al.. (2009). Synthesis and Optical Properties of 2‐(Benzo[b]thiophene‐3‐yl)pyrroles and a New BODIPY Fluorophore (BODIPY=4,4‐Difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene). Chemistry - A European Journal. 15(23). 5823–5830. 41 indexed citations
12.
Афонин, А. В., Igor А. Ushakov, Alexander V. Vashchenko, et al.. (2008). CH···N and CH···O intramolecular hydrogen bonding effects in the 1H, 13C and 15 N NMR spectra of the configurational isomers of 1‐vinylpyrrole‐2‐carbaldehyde oxime substantiated by DFT calculations. Magnetic Resonance in Chemistry. 47(2). 105–112. 39 indexed citations
13.
Афонин, А. В., Igor А. Ushakov, А. Й. Михалева, & Б. А. Трофимов. (2007). Bifurcated hydrogen‐bonding effect on the shielding and coupling constants in trifluoroacetyl pyrroles as studied by 1H, 13C and 15N NMR spectroscopy and DFT calculations. Magnetic Resonance in Chemistry. 45(3). 220–230. 24 indexed citations
14.
Vashchenko, Alexander V., et al.. (2006). The structure of dihydropyrroloindoles: A quantum-chemical estimation of conjugation in cyclohexadiene systems. Journal of Structural Chemistry. 47(4). 616–621. 2 indexed citations
15.
Rusakov, Yury Yu., Leonid B. Krivdin, Elena Yu. Schmidt, А. Й. Михалева, & Б. А. Трофимов. (2006). Nonempirical calculations of NMR indirect spin–spin coupling constants. Part 15: pyrrolylpyridines. Magnetic Resonance in Chemistry. 44(7). 692–697. 13 indexed citations
16.
Rusakov, Yury Yu., Leonid B. Krivdin, Elena Yu. Schmidt, et al.. (2006). Conformational study of 2‐arylazo‐1‐vinylpyrroles. Magnetic Resonance in Chemistry. 45(2). 142–151. 14 indexed citations
17.
Трофимов, Б. А., A. P. Demenev, Lyubov N. Sobenina, А. Й. Михалева, & О. А. Тарасова. (2003). The First Chemoselective Synthesis of Functionalized 3‐Vinylpyrroles.. ChemInform. 34(30). 1 indexed citations
18.
Лебедева, О. В., et al.. (2002). Copolymerization of 1-Vinyl-4,5,6,7-tetrahydroindole with Vinyl Chloride in the Presence of a Radical Initiator. Russian Journal of Applied Chemistry. 75(9). 1462–1464. 1 indexed citations
19.
Трофимов, Б. А., A. P. Demenev, А. Й. Михалева, et al.. (2001). Tricyanovinylpyrroles: synthesis, conformational structure, photosensitizing properties, and electrical conductivity. ARKIVOC. 2001(9). 37–48. 7 indexed citations
20.
Трофимов, Б. А., А. М. Васильцов, Elena Yu. Schmidt, О. В. Петрова, & А. Й. Михалева. (1995). ChemInform Abstract: 2‐Methyl‐3‐alkenylpyrrole from Oximes of Terpenoid Ketones and Acetylene.. ChemInform. 26(30). 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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