Л. М. Алексеева

564 total citations
132 papers, 329 citations indexed

About

Л. М. Алексеева is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Л. М. Алексеева has authored 132 papers receiving a total of 329 indexed citations (citations by other indexed papers that have themselves been cited), including 106 papers in Organic Chemistry, 24 papers in Molecular Biology and 17 papers in Toxicology. Recurrent topics in Л. М. Алексеева's work include Synthesis and Reactions of Organic Compounds (45 papers), Synthesis and Characterization of Heterocyclic Compounds (28 papers) and Synthesis and biological activity (23 papers). Л. М. Алексеева is often cited by papers focused on Synthesis and Reactions of Organic Compounds (45 papers), Synthesis and Characterization of Heterocyclic Compounds (28 papers) and Synthesis and biological activity (23 papers). Л. М. Алексеева collaborates with scholars based in Russia, Bulgaria and Tajikistan. Л. М. Алексеева's co-authors include В. Г. Граник, S. A. Savina, Alexander S. Shashkov, Vadim Makarov, А. С. Шашков, Владимир В. Чернышев, К. И. Кобраков, Г. Н. Петрова, O. B. Ryabova and А. С. Иванов and has published in prestigious journals such as SHILAP Revista de lepidopterología, Tetrahedron and Tetrahedron Letters.

In The Last Decade

Л. М. Алексеева

106 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Л. М. Алексеева Russia	8	281	57	29	29	18	132	329
Ted Judd United States	8	259 0.9×	99 1.7×	50 1.7×	37 1.3×	13 0.7×	10	369
Toshihiko Naito Japan	11	274 1.0×	54 0.9×	23 0.8×	20 0.7×	27 1.5×	39	323
F. A. Ashour Egypt	9	328 1.2×	84 1.5×	29 1.0×	20 0.7×	5 0.3×	21	383
Masahiko Uchiyama Japan	11	312 1.1×	50 0.9×	13 0.4×	34 1.2×	7 0.4×	14	332
Maria Paz Cabal Spain	8	333 1.2×	91 1.6×	57 2.0×	11 0.4×	15 0.8×	10	371
Antonio C. C. Freitas Brazil	10	315 1.1×	56 1.0×	44 1.5×	25 0.9×	9 0.5×	17	375
Pankaj Saraswat India	4	356 1.3×	100 1.8×	30 1.0×	12 0.4×	10 0.6×	6	407
Mouhamad Jida France	14	375 1.3×	178 3.1×	33 1.1×	27 0.9×	13 0.7×	28	426
Yasufumi Wada Japan	11	326 1.2×	40 0.7×	18 0.6×	20 0.7×	20 1.1×	11	367
Varughese Alexander South Korea	10	211 0.8×	147 2.6×	29 1.0×	27 0.9×	17 0.9×	15	348

Countries citing papers authored by Л. М. Алексеева

Since Specialization

Citations

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

Fields of papers citing papers by Л. М. Алексеева

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Л. М. Алексеева. 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 Л. М. Алексеева. The network helps show where Л. М. Алексеева may publish in the future.

Co-authorship network of co-authors of Л. М. Алексеева

This figure shows the co-authorship network connecting the top 25 collaborators of Л. М. Алексеева. A scholar is included among the top collaborators of Л. М. Алексеева 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 Л. М. Алексеева. Л. М. Алексеева 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

Алексеева, Л. М., et al.. (2023). Mobility of Contemporary Terminology. SHILAP Revista de lepidopterología. 12(8). 9–27.

Makarov, Vadim, et al.. (2007). Synthesis of Derivatives of a New Heterocyclic System Pyrazolo[3,4‐b]pyrido[1′,2′:1,2]imidazo[4,5‐d]pyridine.. ChemInform. 38(5). 1 indexed citations

Алексеева, Л. М., et al.. (2007). Synthesis of derivatives of the new heterocyclic system pyrimido[5′,4′:5,6]pyrido[3,2-b]indole. Russian Chemical Bulletin. 56(8). 1588–1594.

Алексеева, Л. М., et al.. (2006). A new method for the synthesis of [1,4]diazepino[6,5-b]indole derivatives. Russian Chemical Bulletin. 55(12). 2278–2284. 2 indexed citations

Алексеева, Л. М., et al.. (2006). A new approach to the synthesis of pyrrolo[1,2-a]indole derivatives. Russian Chemical Bulletin. 55(12). 2271–2277. 1 indexed citations

Алексеева, Л. М., et al.. (2005). Synthesis and antiinflammatory activity of N-[1-(5-R-Oxy-2-methylbenzofuran-3-yl)ethyl]-N-hydroxyureas. Pharmaceutical Chemistry Journal. 39(12). 636–640. 3 indexed citations

Иванов, А. С., et al.. (2003). Functionalization of benzo[b][1,6]naphthyridine derivatives. Russian Chemical Bulletin. 52(5). 1182–1189. 2 indexed citations

Алексеева, Л. М., et al.. (2002). Novel synthesis of chromene and benzofuran derivatives via the Nenitzescu reaction. Mendeleev Communications. 12(1). 15–16. 3 indexed citations

Алексеева, Л. М., et al.. (2002). Synthesis and properties of [1,4]diazepino[6,5-b]indoles. Russian Chemical Bulletin. 51(3). 506–512. 2 indexed citations

10.

Алексеева, Л. М., et al.. (2001). Synthesis and Some Transformations of Derivatives of Pyrido[3,2-b]indole (δ-Carboline). Chemistry of Heterocyclic Compounds. 37(8). 997–1004. 2 indexed citations

11.

Алексеева, Л. М., et al.. (2000). 1H-pyrido[3,2-b]indoles. Synthesis and investigation of some their spectroscopic and chemical properties. Chemistry of Heterocyclic Compounds. 36(3). 301–306. 4 indexed citations

12.

Алексеева, Л. М., et al.. (1998). New approach to synthesis of derivatives of 2-(5-hydroxybenzofuryl-3)naphthofurans. Chemistry of Heterocyclic Compounds. 34(6). 651–657. 3 indexed citations

13.

Алексеева, Л. М., et al.. (1995). Synthesis of Functionally-substituted Dienediamines and some Chemical Transformations. Mendeleev Communications. 5(1). 24–25. 6 indexed citations

14.

Алексеева, Л. М., et al.. (1995). Synthesis and biological activity of dienediaminoketones of the indolin-3-one and 2-pyrrolin-4-one series. Pharmaceutical Chemistry Journal. 29(9). 610–617. 2 indexed citations

15.

Алексеева, Л. М., et al.. (1992). Lactam and acid amide acetals. 71. New synthesis of 3-nitro-6-hydroxyindole derivatives. Chemistry of Heterocyclic Compounds. 28(1). 34–39. 4 indexed citations

16.

Алексеева, Л. М., et al.. (1990). Rearrangement of 1-acetylindoxyl oxime into 1-acetyl-2-acetoxy-3-iminoindoline hydrosulfate. Chemistry of Heterocyclic Compounds. 26(3). 279–281. 1 indexed citations

17.

Алексеева, Л. М., et al.. (1987). Synthesis and antimicrobial activity of 5-hydroxynaphtho[1,2-b] thiophenes and 4-hydroxybenzo[2,1-b∶3,4-b']dithiophenes. Pharmaceutical Chemistry Journal. 21(11). 772–777. 1 indexed citations

18.

Алексеева, Л. М., et al.. (1986). Azo coupling and aminomethylation of 2,5-diphenylpyrrole and its derivatives. Chemistry of Heterocyclic Compounds. 22(5). 499–503. 2 indexed citations

19.

Алексеева, Л. М., et al.. (1983). Preparation of 16-substituted 3-hydroxyestra-1,3,5(10)-triene-17-ones starting with the bromination of estrone acetate. Chemistry of Natural Compounds. 19(4). 437–440. 2 indexed citations

20.

Jones, Richard A., et al.. (1970). The electrophilic substitution of benzoquinuclidine. Tetrahedron Letters. 11(21). 1809–1812. 1 indexed citations

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