E. D. Matveeva

975 total citations
61 papers, 758 citations indexed

About

E. D. Matveeva is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, E. D. Matveeva has authored 61 papers receiving a total of 758 indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Organic Chemistry, 12 papers in Molecular Biology and 11 papers in Pharmaceutical Science. Recurrent topics in E. D. Matveeva's work include Oxidative Organic Chemistry Reactions (19 papers), Organophosphorus compounds synthesis (17 papers) and Catalytic C–H Functionalization Methods (12 papers). E. D. Matveeva is often cited by papers focused on Oxidative Organic Chemistry Reactions (19 papers), Organophosphorus compounds synthesis (17 papers) and Catalytic C–H Functionalization Methods (12 papers). E. D. Matveeva collaborates with scholars based in Russia, Tajikistan and Germany. E. D. Matveeva's co-authors include Н. С. Зефиров, N. S. Zefirov, Tatyana A. Podrugina, Rolf Gleiter, А. В. Миронов, М. В. Проскурнина, T. D. Nekipelova, Larisa G. Tomilova, Viktor V. Zhdankin and V. A. Kuz’min and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Tetrahedron Letters.

In The Last Decade

E. D. Matveeva

58 papers receiving 733 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. D. Matveeva Russia 17 705 98 62 55 48 61 758
Richard H. Wettach United States 12 767 1.1× 168 1.7× 55 0.9× 43 0.8× 59 1.2× 15 821
Joanna T. Negri United States 15 407 0.6× 91 0.9× 96 1.5× 62 1.1× 19 0.4× 18 481
Damien Belotti France 16 531 0.8× 72 0.7× 125 2.0× 18 0.3× 36 0.8× 33 591
Gergely L. Tolnai Hungary 13 768 1.1× 89 0.9× 96 1.5× 54 1.0× 127 2.6× 20 828
Andrée Parlier France 17 673 1.0× 102 1.0× 41 0.7× 20 0.4× 56 1.2× 46 715
Steven W. Tregay United States 6 474 0.7× 185 1.9× 86 1.4× 17 0.3× 33 0.7× 6 525
Karen E. Torraca United States 8 628 0.9× 138 1.4× 98 1.6× 34 0.6× 35 0.7× 9 694
Tracy Yuen Sze But Hong Kong 7 422 0.6× 82 0.8× 187 3.0× 34 0.6× 28 0.6× 10 493
Karl Matos Puerto Rico 8 760 1.1× 252 2.6× 158 2.5× 60 1.1× 21 0.4× 15 859
Hidenori Chikashita Japan 16 509 0.7× 97 1.0× 138 2.2× 28 0.5× 35 0.7× 42 588

Countries citing papers authored by E. D. Matveeva

Since Specialization
Citations

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

Fields of papers citing papers by E. D. Matveeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. D. Matveeva

This figure shows the co-authorship network connecting the top 25 collaborators of E. D. Matveeva. A scholar is included among the top collaborators of E. D. Matveeva 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 E. D. Matveeva. E. D. Matveeva 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.
Kuz’min, V. A., T. D. Nekipelova, М. В. Проскурнина, et al.. (2016). New phosphonate-substituted tricarbocyanines and their interaction with bovine serum albumin. Doklady Chemistry. 470(1). 264–267. 3 indexed citations
2.
Kuz’min, V. A., Nikita A. Durandin, T. D. Nekipelova, et al.. (2015). Energy degradation in photoexcited complexes of indocarbocyanine with albumin. High Energy Chemistry. 49(3). 211–212. 7 indexed citations
3.
Kuz’min, V. A., Nikita A. Durandin, T. D. Nekipelova, et al.. (2015). Spectral and kinetic characteristics of indotricarbocyanine complexation with albumin. Doklady Physical Chemistry. 462(1). 107–109. 5 indexed citations
4.
Matveeva, E. D., et al.. (2013). Phosphonium-Iodonium Ylides with Heteroatomic Groups in the Synthesis of Annelated P-Containing Heterocycles. The Journal of Organic Chemistry. 78(23). 11691–11697. 20 indexed citations
5.
6.
Matveeva, E. D., et al.. (2009). Aminopyridines as amino components in the catalytic synthesis of α-aminophosphonates. Russian Chemical Bulletin. 58(1). 119–125. 5 indexed citations
7.
Matveeva, E. D., et al.. (2008). One-pot process in phosphonium-iodonium ylides: nucleophilic substitution and the Wittig reaction. Russian Chemical Bulletin. 57(2). 400–405. 14 indexed citations
8.
Matveeva, E. D., et al.. (2007). Three-component catalytic method for synthesis of α-amino phosphonates with the use of α-amino acids as amine component. Russian Chemical Bulletin. 56(4). 798–805. 9 indexed citations
9.
Matveeva, E. D., М. В. Проскурнина, & Н. С. Зефиров. (2006). Polyvalent iodine in organic chemistry: Recent developments, 2002–2005. Heteroatom Chemistry. 17(6). 595–617. 33 indexed citations
10.
Matveeva, E. D. & Н. С. Зефиров. (2006). Amino acids in a three-component synthesis of α-aminophosphonates derivatives. Russian Journal of Organic Chemistry. 42(8). 1237–1238. 10 indexed citations
11.
Matveeva, E. D., et al.. (2006). Chemo-and stereoselectivity of the reaction of aromatic aldehydes with triphenylphosphine and trichloroacetic acid derivatives. Russian Journal of Organic Chemistry. 42(3). 388–392. 1 indexed citations
12.
Matveeva, E. D., O. N. Zefirova, И. В. Серегин, et al.. (2002). Syntheses of Compounds Active toward Glutamate Receptors: II. Synthesis of Spiro Hydantoins of the Indan Series. Russian Journal of Organic Chemistry. 38(12). 1769–1774. 4 indexed citations
13.
Matveeva, E. D., O. N. Zefirova, А.С. Алексеев, et al.. (2002). Syntheses of Compounds Active toward Glutamate Receptors: I. New Preparative Synthesis of Aminoindandicarboxylic Acid (AIDA). Russian Journal of Organic Chemistry. 38(12). 1764–1768. 1 indexed citations
14.
Matveeva, E. D., et al.. (2000). Stereodirectional synthesis of the main component of pheromone (9Z,12E)-tetradeca-9,12-dienyl acetate by cross-coupling. Russian Journal of Electrochemistry. 36(6). 765–770. 1 indexed citations
15.
Matveeva, E. D., et al.. (2000). Synthesis and Neuroprotective Properties of Isosteric Analogs of Nicotine. Chemistry of Heterocyclic Compounds. 36(10). 1149–1153. 1 indexed citations
16.
Matveeva, E. D., et al.. (1995). Regioselective and stereoselective substitution of hydroxyl group for halogen in allyl alcohols. Zhurnal Organicheskoi Khimii. 31(8). 1121–1125. 2 indexed citations
17.
Matveeva, E. D., et al.. (1989). REGIOSPECIFIC AND STEREOSPECIFIC SUBSTITUTION OF HYDROXYL OF ALIPHATIC-ALCOHOLS WITH HALOGEN. Zhurnal Organicheskoi Khimii. 25(4). 716–721. 3 indexed citations
18.
Matveeva, E. D., et al.. (1986). The Synthesis of Lepidoptera Pheromones. Russian Chemical Reviews. 55(7). 672–689. 9 indexed citations
19.
Matveeva, E. D., et al.. (1980). SYNTHESIS OF HIGHER ACETYLENIC ALCOHOLS. Zhurnal Organicheskoi Khimii. 16(10). 2032–2038. 5 indexed citations
20.
Кост, А. Н., et al.. (1970). ISOMERIZATION OF Z-SUBSTITUTED INDOLES, BENZOFURANS AND BENZOTHIOFURANS. Zhurnal Organicheskoi Khimii. 6(7). 1503. 10 indexed citations

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