М. И. Кодесс

3.1k total citations
291 papers, 2.5k citations indexed

About

М. И. Кодесс is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, М. И. Кодесс has authored 291 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 248 papers in Organic Chemistry, 101 papers in Pharmaceutical Science and 51 papers in Molecular Biology. Recurrent topics in М. И. Кодесс's work include Synthesis and Reactions of Organic Compounds (113 papers), Fluorine in Organic Chemistry (98 papers) and Synthesis and Biological Evaluation (96 papers). М. И. Кодесс is often cited by papers focused on Synthesis and Reactions of Organic Compounds (113 papers), Fluorine in Organic Chemistry (98 papers) and Synthesis and Biological Evaluation (96 papers). М. И. Кодесс collaborates with scholars based in Russia, Belgium and Germany. М. И. Кодесс's co-authors include Vyacheslav Ya. Sosnovskikh, Марина А. Ежикова, Valery N. Charushin, Олег Н. Чупахин, Павел А. Слепухин, Vladislav Yu. Korotaev, В. П. Краснов, Владимир С. Мошкин, В. И. Салоутин and Галина Л. Левит and has published in prestigious journals such as SHILAP Revista de lepidopterología, Carbohydrate Polymers and Electrochimica Acta.

In The Last Decade

М. И. Кодесс

264 papers receiving 2.4k citations

Peers

М. И. Кодесс

PHARM

SPECT

Janez Košmrlj Slovenia

L. R. Subramanian Germany

Akio Kamimura Japan

Adinath Majee India

Kyung Woon Jung United States

Attila Bényei Hungary

Robert E. Maleczka United States

Lidia De Luca Italy

Damien Prim France

А. Й. Михалева Russia

Janez Košmrlj Slovenia

М. И. Кодесс

1.9k ×0.9

535 ×1.1

107 ×0.2

102 ×0.3

PHARM

84 ×0.5

SPECT

Citations per year, relative to М. И. Кодесс М. И. Кодесс (= 1×) peers Janez Košmrlj

Countries citing papers authored by М. И. Кодесс

Since Specialization

Citations

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

Fields of papers citing papers by М. И. Кодесс

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of М. И. Кодесс

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

Gruzdev, Dmitry А., et al.. (2025). Synthesis of carborane-containing glycerides as boron-rich lipid analogues. Journal of Organometallic Chemistry. 1039. 123813–123813.

Gruzdev, Dmitry А., Марина А. Ежикова, М. И. Кодесс, et al.. (2024). Synthesis of novel zwitterionic nido-carborane-containing derivatives of cysteine and methionine. Russian Chemical Bulletin. 73(6). 1716–1724. 2 indexed citations

Burgart, Yanina V., et al.. (2023). A New Efficient One‐Pot Three‐Component Synthesis of Diverse Pyrido[1,2‐ a ]pyrimidines. ChemistrySelect. 8(43). 1 indexed citations

Burgart, Yanina V., et al.. (2023). Multicomponent Domino Cyclization of Ethyl Trifluoropyruvate with Methyl Ketones and Amino Alcohols as A New Way to γ-Lactam Annulated Oxazacycles. Molecules. 28(4). 1983–1983.

Gruzdev, Dmitry А., et al.. (2023). Synthesis of Charge-Compensated nido-Carboranyl Derivatives of Sulfur-Containing Amino Acids and Biotin. The Journal of Organic Chemistry. 88(19). 14022–14032. 4 indexed citations

Краснов, В. П., Галина Л. Левит, М. И. Кодесс, et al.. (2023). Synthesis and Assessment of Antiplatelet and Antithrombotic Activity of 4-Amino-Substituted 5-Oxoproline Amides and Peptides. Molecules. 28(21). 7401–7401.

Кодесс, М. И., et al.. (2023). Kinetic resolution of racemic 6-substituted 3-methyl-3,4-dihydro-2H-[1,4]benzoxazines with chiral acyl chlorides. Russian Chemical Bulletin. 72(12). 2938–2947. 1 indexed citations

Кодесс, М. И., et al.. (2023). Two-step synthesis of indeno[1,2-b]furazanopyrazines through combination of the SNH and Heck reactions. Mendeleev Communications. 33(6). 753–755. 2 indexed citations

Gorbunov, Evgeny B., et al.. (2022). Synthesis of purine conjugates with N-(4-aminobenzenesulfonyl)-and N-(2-aminoethanesulfonyl)-(S)-glutamic acids. Russian Chemical Bulletin. 71(12). 2685–2690. 1 indexed citations

10.

Burgart, Yanina V., Марина А. Ежикова, М. И. Кодесс, et al.. (2021). New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity. Organic & Biomolecular Chemistry. 19(45). 9925–9935. 7 indexed citations

11.

Burgart, Yanina V., et al.. (2021). Multicomponent Domino Reactions for the Synthesis of Variable Hydrogenated Imidazo[1,2‐a]pyridines. Asian Journal of Organic Chemistry. 11(2). 8 indexed citations

12.

Худина, О. Г., Yanina V. Burgart, Yulia S. Kudyakova, et al.. (2019). Autocatalyzed three-component cyclization of polyfluoroalkyl-3-oxo esters, methyl ketones and alkyl amines: a novel approach to 3-alkylamino-5-hydroxy-5-polyfluoroalkylcyclohex-2-en-1-ones. Organic & Biomolecular Chemistry. 17(17). 4273–4280. 9 indexed citations

13.

Burgart, Yanina V., et al.. (2017). Synthesis of Pyridone Derivatives from 7‐Hydroxy‐7‐polyfluoroalkylhexahydroimidazo[1,2‐a]pyridin‐5‐ones. European Journal of Organic Chemistry. 2017(27). 3986–3991. 8 indexed citations

14.

Burgart, Yanina V., et al.. (2015). The reactions of 2-ethoxymethylidene-3-oxo esters and their analogues with 5-aminotetrazole as a way to novel azaheterocycles. Beilstein Journal of Organic Chemistry. 11. 385–391. 16 indexed citations

15.

Bakulev, Vasiliy А., et al.. (2015). Synthesis of pyrido[2,3-d]pyrimidines from 6-amino-1,3-dimethyluracil and aldehydes. Russian Journal of Organic Chemistry. 51(12). 1784–1787. 1 indexed citations

16.

Pestov, Alexander V., et al.. (2015). Imidazolyl derivative of chitosan with high substitution degree: Synthesis, characterization and sorption properties. Carbohydrate Polymers. 138. 252–258. 18 indexed citations

17.

Кодесс, М. И., et al.. (2003). Reaction of 5-halo-1,2,3-thiadiazoles with aliphatic diamines. Synthesis and intramolecular cyclization of bis(1,2,3-triazolyl-1,2,3-thiadiazolyl)sulfides. Organic & Biomolecular Chemistry. 1(22). 4030–4030. 6 indexed citations

18.

Краснов, В. П., et al.. (2002). Synthesis of ( 2S, 4S)-4-phenylamino-5-oxoproline derivatives.. Amino Acids. 22(2). 179–186. 7 indexed citations

19.

Charushin, Valery N., Emiliya V. Nosova, G. N. Lipunova, & М. И. Кодесс. (2001). Fused fluoroquinolones: synthesis and 1H and 19F NMR studies. Journal of Fluorine Chemistry. 110(1). 25–30. 9 indexed citations

20.

Кодесс, М. И., et al.. (1988). Stereochemistry of the epoxidation of internal perfluoroalkenes with sodium hypochlorite. 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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