Л. В. Спирихин

1.8k total citations
315 papers, 1.4k citations indexed

About

Л. В. Спирихин is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Л. В. Спирихин has authored 315 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 203 papers in Organic Chemistry, 112 papers in Molecular Biology and 37 papers in Pharmacology. Recurrent topics in Л. В. Спирихин's work include Natural product bioactivities and synthesis (45 papers), Carbohydrate Chemistry and Synthesis (31 papers) and Synthetic Organic Chemistry Methods (26 papers). Л. В. Спирихин is often cited by papers focused on Natural product bioactivities and synthesis (45 papers), Carbohydrate Chemistry and Synthesis (31 papers) and Synthetic Organic Chemistry Methods (26 papers). Л. В. Спирихин collaborates with scholars based in Russia, Austria and Hungary. Л. В. Спирихин's co-authors include Marat S. Yunusov, Г. А. Толстиков, И. Б. Абдрахманов, А. Н. Лобов, Л. А. Балтина, Р. Р. Гатауллин, Ф. З. Галин, Ф. А. Валеев, А. А. Фатыхов and С. Л. Хурсан and has published in prestigious journals such as Tetrahedron, The Journal of Physical Chemistry A and Tetrahedron Letters.

In The Last Decade

Л. В. Спирихин

268 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Л. В. Спирихин Russia	15	793	594	189	97	94	315	1.4k
Paulo Marcos Donate Brazil	19	339 0.4×	355 0.6×	101 0.5×	98 1.0×	76 0.8×	70	954
Pedro de March Spain	26	1.7k 2.1×	396 0.7×	153 0.8×	97 1.0×	127 1.4×	110	2.0k
Giancarlo Fantin Italy	26	1.1k 1.4×	905 1.5×	125 0.7×	173 1.8×	112 1.2×	130	2.0k
Ramón J. Zaragozá Spain	20	950 1.2×	289 0.5×	77 0.4×	52 0.5×	113 1.2×	82	1.3k
Dieter Ströhl Germany	21	547 0.7×	488 0.8×	145 0.8×	71 0.7×	112 1.2×	70	1.1k
Ningbo Gong China	22	376 0.5×	627 1.1×	135 0.7×	225 2.3×	95 1.0×	80	1.3k
Qing‐Shan Li China	27	1.3k 1.7×	401 0.7×	165 0.9×	167 1.7×	53 0.6×	103	2.1k
Vyacheslav E. Semenov Russia	18	765 1.0×	423 0.7×	62 0.3×	103 1.1×	191 2.0×	133	1.2k
Jingbo Yu China	22	977 1.2×	315 0.5×	129 0.7×	162 1.7×	52 0.6×	59	1.6k
Tadashi Tsuda Japan	17	328 0.4×	392 0.7×	63 0.3×	131 1.4×	61 0.6×	85	979

Countries citing papers authored by Л. В. Спирихин

Since Specialization

Citations

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

Fields of papers citing papers by Л. В. Спирихин

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Л. В. Спирихин

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

Khusnutdinova, E. F., et al.. (2024). Messagenin–based Chalcones: Synthesis, Modification and Perspectives of Antidiabetic Potency. Asian Journal of Organic Chemistry. 13(6). 1 indexed citations

Раскильдина, Г. З., et al.. (2024). Effect of Solvents on the Conformational Preferences of Oxy[bis(methylene)]bis[(1,3-dioxan-5-yl)methanol]. Russian Journal of Organic Chemistry. 60(2). 198–205.

Спирихин, Л. В., et al.. (2024). Synthesis of Nitrones Based on Triterpenes C<sup>3</i>-Hydroxylamines of the Lupane Series. Журнал Общей Химии. 94(7). 805–814.

Спирихин, Л. В., et al.. (2023). Synthesis of New Amidoethanesulfonamides of Betulonic Acid. Chemistry of Natural Compounds. 59(2). 313–317.

Лобов, А. Н., et al.. (2022). Hydrogels on the Base of Modified Chitosan and Hyaluronic Acid Mix as Polymer Matrices for Cytostatics Delivery. Gels. 8(2). 104–104. 14 indexed citations

Раскильдина, Г. З., et al.. (2019). SYNTHESIS AND PHYSICAL AND CHEMICAL CHARACTERISTICS OF ISOMERIC 2-, 4-SUBSTITUTED 1,3-DIOXACYCLOALCANES. 4–12. 2 indexed citations

Лобов, А. Н., et al.. (2014). 5-Fluorouracil solutions: NMR study of acid-base equilibrium in water and DMSO. Journal of Physical Organic Chemistry. 27(11). 876–883. 35 indexed citations

Казакова, О. Б., E. F. Khusnutdinova, А. Н. Лобов, Н. И. Медведева, & Л. В. Спирихин. (2011). Allylic oxidation of 19β,28-epoxy-a-neo-5β-methyl-25-nor-18α-olean-9-ene. Chemistry of Natural Compounds. 47(4). 579–582. 3 indexed citations

Казакова, О. Б., et al.. (2010). The synthesis and anti-inflammatory activity of quinopimaric acid derivatives. Russian Journal of Bioorganic Chemistry. 36(2). 257–262. 25 indexed citations

10.

Куковинец, О. С., et al.. (2006). Novel synthesis of Planococcus citri pheromone. Chemistry of Natural Compounds. 42(2). 216–218. 6 indexed citations

11.

Фатыхов, А. А., et al.. (2006). Double α-ketol rearrangement of (−)-1-{(1S,2R,4R)-1-ethenyl-2-hydroxy-7,7-dimethylbicyclo[2.2.1]hept-2-yl}ethan-1-one. Russian Journal of Organic Chemistry. 42(6). 839–843. 1 indexed citations

12.

Спирихин, Л. В., et al.. (2005). Cyclopropanation of betulonic acid and its methyl ester with dichlorocarbene generated under phase transfer catalysis conditions. Russian Chemical Bulletin. 54(11). 2659–2663. 4 indexed citations

13.

Спирихин, Л. В., et al.. (2003). Synthesis of a Ring Fragment of 9α,11α-Thiathromboxane A2. Procedure for Bond C1-C2 Cleavage in Monosaccharides by an Example of D-Glucose 2-Deoxy-3-mesyl Derivative. Russian Journal of Organic Chemistry. 39(6). 834–836.

14.

Спирихин, Л. В., et al.. (2003). 16-Demethoxymethyllycaconitine, a new norditerpenoid alkaloid from Delphinium cuneatum. Russian Chemical Bulletin. 52(9). 2078–2080. 2 indexed citations

15.

Муслухов, Р. Р., et al.. (2002). Four Main Reduced Forms of Polydiphenylenesulfophthalide. Doklady Physical Chemistry. 387(4-6). 320–323. 1 indexed citations

16.

Флехтер, О. Б., Л. А. Балтина, Ф. С. Зарудий, et al.. (2002). Synthesis and Pharmacological Activity of Betulin Dinicotinate. Russian Journal of Bioorganic Chemistry. 28(6). 494–500. 22 indexed citations

17.

Мустафин, А. Г., Р. Р. Гатауллин, Л. В. Спирихин, И. Б. Абдрахманов, & Г. А. Толстиков. (1997). ChemInform Abstract: Transformations of β‐D‐Xylofuranosylnucleosides. Synthesis of 3′‐ Deoxy‐2′,3′‐didehydrothymidine (D4T).. ChemInform. 28(29). 1 indexed citations

18.

Tolstikov, A. G., et al.. (1993). A Short Route to Chiral Synthons: Preparation of Ketoeicosanoids with Hydropyrane Fragments. Mendeleev Communications. 3(1). 18–20.

19.

Толстиков, А. Г., et al.. (1991). (9R,12R,13R,5Z,10Z)‐12‐アセトキシ‐9,13‐オキサ‐5,10‐オクタデカジエン酸のエナンチオ特異的合成. Zhurnal Organicheskoi Khimii. 27(4). 879–880.

20.

Спирихин, Л. В., et al.. (1976). チオアルキル化反応 I アルカンチオールによるケトンのチオアルキル化. Zhurnal Organicheskoi Khimii. 12(8). 1672–1676. 2 indexed citations

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