Д. В. Корчагина

2.5k total citations
183 papers, 2.1k citations indexed

About

Д. В. Корчагина is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Д. В. Корчагина has authored 183 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Organic Chemistry, 67 papers in Molecular Biology and 21 papers in Spectroscopy. Recurrent topics in Д. В. Корчагина's work include Synthetic Organic Chemistry Methods (31 papers), Asymmetric Synthesis and Catalysis (22 papers) and Chemical Synthesis and Reactions (18 papers). Д. В. Корчагина is often cited by papers focused on Synthetic Organic Chemistry Methods (31 papers), Asymmetric Synthesis and Catalysis (22 papers) and Chemical Synthesis and Reactions (18 papers). Д. В. Корчагина collaborates with scholars based in Russia, New Zealand and Finland. Д. В. Корчагина's co-authors include Нариман Ф. Салахутдинов, Константин П. Волчо, И. В. Ильина, V. A. Barkhash, Е. В. Суслов, А.В. Павлова, Т. Г. Толстикова, Т. М. Хоменко, Н. И. Комарова and Oleg V. Ardashov and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Journal of Medicinal Chemistry.

In The Last Decade

Д. В. Корчагина

177 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Д. В. Корчагина Russia 25 1.1k 831 333 275 237 183 2.1k
Gábor Tóth Hungary 26 1.2k 1.2× 1.2k 1.4× 263 0.8× 233 0.8× 212 0.9× 230 2.9k
Charles B. de Koning South Africa 32 2.8k 2.6× 783 0.9× 247 0.7× 145 0.5× 325 1.4× 133 3.3k
Gustavo Seoane Uruguay 21 1.3k 1.2× 706 0.8× 229 0.7× 97 0.4× 155 0.7× 111 2.0k
Pallab Pahari India 24 1.3k 1.2× 664 0.8× 609 1.8× 145 0.5× 146 0.6× 57 2.0k
A. V. R. RAO India 27 1.6k 1.5× 846 1.0× 393 1.2× 242 0.9× 324 1.4× 154 2.5k
Lothar Hennig Germany 24 1.1k 1.0× 766 0.9× 364 1.1× 190 0.7× 153 0.6× 179 2.2k
Sylvie Ducki United Kingdom 27 1.6k 1.5× 809 1.0× 341 1.0× 122 0.4× 77 0.3× 55 2.4k
Marta Ferraroni Italy 32 1.1k 1.0× 1.8k 2.1× 544 1.6× 152 0.6× 267 1.1× 110 2.6k
Nabin C. Barua India 26 1.6k 1.5× 949 1.1× 166 0.5× 128 0.5× 322 1.4× 105 2.6k
Hisahiro Hagiwara Japan 31 2.7k 2.5× 701 0.8× 279 0.8× 394 1.4× 362 1.5× 199 3.6k

Countries citing papers authored by Д. В. Корчагина

Since Specialization
Citations

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

Fields of papers citing papers by Д. В. Корчагина

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Д. В. Корчагина

This figure shows the co-authorship network connecting the top 25 collaborators of Д. В. Корчагина. A scholar is included among the top collaborators of Д. В. Корчагина 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 Д. В. Корчагина. Д. В. Корчагина 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.
Ившина, И. Б., Константин П. Волчо, Yu. V. Gatilov, et al.. (2022). Biotransformation of (–)-Isopulegol by Rhodococcus rhodochrous. Pharmaceuticals. 15(8). 964–964. 7 indexed citations
2.
Sidorenko, A.Yu., Päivi Mäki‐Arvela, Atte Aho, et al.. (2020). Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes. Molecular Catalysis. 490. 110974–110974. 14 indexed citations
3.
Ильина, И. В., Nadezhda S. Dyrkheeva, Alexandra L. Zakharenko, et al.. (2020). Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1. Molecules. 25(15). 3496–3496. 28 indexed citations
4.
Хоменко, Т. М., Alexandra L. Zakharenko, Arina A. Chepanova, et al.. (2019). Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy. International Journal of Molecular Sciences. 21(1). 126–126. 39 indexed citations
5.
Павлова, А.В., et al.. (2017). Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2-Chromen-4,8-Diols Containing Alkyl-Substituted Aromatic Moieties. Chemistry of Natural Compounds. 53(6). 1066–1071. 1 indexed citations
6.
Суслов, Е. В., Владимир В. Зарубаев, Alexander V. Slita, et al.. (2017). Anti-influenza activity of diazaadamantanes combined with monoterpene moieties. Bioorganic & Medicinal Chemistry Letters. 27(19). 4531–4535. 16 indexed citations
7.
Зарубаев, Владимир В., et al.. (2016). Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes. Bioorganic & Medicinal Chemistry. 24(21). 5158–5161. 34 indexed citations
8.
Ильина, И. В., Аndrey G. Pokrovsky, Д. В. Корчагина, et al.. (2015). Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (–)-verbenone. Russian Chemical Bulletin. 64(9). 2257–2260. 1 indexed citations
9.
Соколова, А. С., Оlga I. Yarovaya, Д. В. Корчагина, et al.. (2014). Camphor-based symmetric diimines as inhibitors of influenza virus reproduction. Bioorganic & Medicinal Chemistry. 22(7). 2141–2148. 44 indexed citations
10.
Salomatina, Oksana V., Andrey V. Markov, Д. В. Корчагина, et al.. (2013). Synthesis of novel 2-cyano substituted glycyrrhetinic acid derivatives as inhibitors of cancer cells growth and NO production in LPS-activated J-774 cells. Bioorganic & Medicinal Chemistry. 22(1). 585–593. 27 indexed citations
11.
Ardashov, Oleg V., et al.. (2013). 3-Methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol: the Importance of Functional Groups for Antiparkinsonian Activity. Medicinal Chemistry. 9(5). 731–739. 10 indexed citations
12.
Суслов, Е. В., Д. В. Корчагина, Н. И. Комарова, et al.. (2012). Synthesis and anxiolytic activity of 2-aminoadamantane derivatives containing monoterpene fragments. Pharmaceutical Chemistry Journal. 46(5). 263–265. 24 indexed citations
13.
Ильина, И. В., Константин П. Волчо, Д. В. Корчагина, et al.. (2010). Unusual Reactions of (+)‐Car‐2‐ene and (+)‐Car‐3‐ene with Aldehydes on K10 Clay. Helvetica Chimica Acta. 93(11). 2135–2150. 17 indexed citations
14.
Ильина, И. В., Д. В. Корчагина, Константин П. Волчо, Нариман Ф. Салахутдинов, & Г. А. Толстиков. (2010). Reaction of sabinene with aldehydes in the presence of montmorillonite K10 clay. Russian Journal of Organic Chemistry. 46(7). 1002–1005. 8 indexed citations
15.
Shernyukov, Аndrey V., et al.. (2009). Spirocyclization of 2,3-seco-19β,28-epoxy-28-oxo-18α-olean-2,3-dicarboxylic anhydride with benzylamines. Doklady Chemistry. 429(1). 286–289. 4 indexed citations
16.
Половинка, М. П., et al.. (2008). Low-molecular-weight phenolic compounds from Hedysarum theinum roots. Chemistry of Natural Compounds. 44(1). 31–34. 31 indexed citations
17.
Salomatina, Oksana V., Оlga I. Yarovaya, Д. В. Корчагина, М. П. Половинка, & V. A. Barkhash. (2005). Solid acid-catalysed isomerization of R(+)-limonene diepoxides. Mendeleev Communications. 15(2). 59–61. 5 indexed citations
18.
Половинка, М. П., et al.. (1998). MOLECULAR REARRANGEMENTS OF ALPHA -(TRANS)- AND BETA -(CIS)-3,4-EPOXYCARANES IN ACID MEDIA. Russian Journal of Organic Chemistry. 34(9). 1283–1291. 2 indexed citations
19.
Половинка, М. П., et al.. (1998). Молекулярные перегруппировки α‐(транс)‐ и β‐(цис)‐3,4‐эпоксикаранов в кислотных средах.. Zhurnal Organicheskoi Khimii. 34(9). 1342–1349. 1 indexed citations
20.
Vlad, P. F., Nicon Ungur, Alic Barbă, et al.. (1991). Superacid isomerization of phylloclandene, isophylloclandene, and phylloclandanol. Chemistry of Natural Compounds. 27(3). 301–308. 1 indexed citations

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