Grigory Kantin

752 total citations
67 papers, 562 citations indexed

About

Grigory Kantin is a scholar working on Organic Chemistry, Molecular Biology and Cancer Research. According to data from OpenAlex, Grigory Kantin has authored 67 papers receiving a total of 562 indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Organic Chemistry, 9 papers in Molecular Biology and 8 papers in Cancer Research. Recurrent topics in Grigory Kantin's work include Cyclopropane Reaction Mechanisms (46 papers), Synthesis and Catalytic Reactions (28 papers) and Catalytic C–H Functionalization Methods (26 papers). Grigory Kantin is often cited by papers focused on Cyclopropane Reaction Mechanisms (46 papers), Synthesis and Catalytic Reactions (28 papers) and Catalytic C–H Functionalization Methods (26 papers). Grigory Kantin collaborates with scholars based in Russia, Germany and Italy. Grigory Kantin's co-authors include Mikhail Krasavin, Dmitry Dar’in, Olga Bakulina, Evgeny Chupakhin, Vladimir V. Sharoyko, Alexander S. Novikov, Alexander S. Bunev, Михаил С. Новиков, Matthis Synofzik and Daniil Zhukovsky and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Chemistry - A European Journal.

In The Last Decade

Grigory Kantin

65 papers receiving 550 citations

Peers

Grigory Kantin
Karen Mollet Belgium
Darren Stead United Kingdom
Dawn M. Troast United States
Yun Liao China
Guillermo S. Cortez United States
Karen Mollet Belgium
Grigory Kantin
Citations per year, relative to Grigory Kantin Grigory Kantin (= 1×) peers Karen Mollet

Countries citing papers authored by Grigory Kantin

Since Specialization
Citations

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

Fields of papers citing papers by Grigory Kantin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Grigory Kantin. 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 Grigory Kantin. The network helps show where Grigory Kantin may publish in the future.

Co-authorship network of co-authors of Grigory Kantin

This figure shows the co-authorship network connecting the top 25 collaborators of Grigory Kantin. A scholar is included among the top collaborators of Grigory Kantin 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 Grigory Kantin. Grigory Kantin 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.
Bunev, Alexander S., Alexander Sapegin, Dmitry Dar’in, et al.. (2025). Extending the chemical space of glutarimide-based cereblon ligands through an efficient Rh(II)-catalyzed X–H insertion reaction. European Journal of Medicinal Chemistry. 301. 118235–118235. 1 indexed citations
2.
Kantin, Grigory, Dmitry Dar’in, Alexander S. Bunev, et al.. (2025). Synthesis of α-(azidomethyl)glutarimide and its applicationin construction of potential Cereblon ligands <em>via</em> the CuAAC reaction. Mendeleev Communications. 35(1). 69–72.
3.
Sapegin, Alexander, et al.. (2024). Discovery and characterization of potent spiro-isoxazole-based cereblon ligands with a novel binding mode. European Journal of Medicinal Chemistry. 270. 116328–116328. 3 indexed citations
4.
Kantin, Grigory, et al.. (2024). Entry to new spiroheterocycles via tandem Rh(II)-catalyzed O–H insertion/base-promoted cyclization involving diazoarylidene succinimides. Beilstein Journal of Organic Chemistry. 20. 561–569. 1 indexed citations
5.
Kantin, Grigory, et al.. (2024). Access to 2-oxoazetidine-3-carboxylic acid derivatives via thermal microwave-assisted Wolff rearrangement of 3-diazotetramic acids in the presence of nucleophiles. Beilstein Journal of Organic Chemistry. 20. 1894–1899. 1 indexed citations
6.
Kantin, Grigory, et al.. (2024). Facile N‐Modification of NH‐Tetrazoles via Rh(II)‐Catalyzed N−H Insertion Involving Structurally Diverse Diazo Reagents. European Journal of Organic Chemistry. 28(4). 1 indexed citations
7.
Kantin, Grigory, Alexander Sapegin, & Dmitry Dar’in. (2024). 5-Diazo Dihydrouracils: Preparation and Some Transformations. The Journal of Organic Chemistry. 89(20). 15197–15205.
8.
Kantin, Grigory, et al.. (2023). Rh(II)-catalyzed condensation of 3-diazotetramic acids with nitriles delivers novel druglike 5,6-dihydro-4H-pyrrolo[3,4-d]oxazol-4-ones. Tetrahedron Letters. 120. 154457–154457. 2 indexed citations
9.
Rodionov, Ivan A., et al.. (2023). Catalyst Loading Controls Chemoselectivity: Unusual Effect in Rhodium(II) Carbene Insertion Reactions with Tetrahydrofuran. Catalysts. 13(2). 428–428. 1 indexed citations
10.
Kantin, Grigory, et al.. (2023). N -Boc-α-diazo glutarimide as efficient reagent for assembling N-heterocycle-glutarimide diads via Rh(II)-catalyzed N–H insertion reaction. Beilstein Journal of Organic Chemistry. 19. 1841–1848. 2 indexed citations
11.
Dar’in, Dmitry, et al.. (2022). A novel spirocyclic scaffold accessed via tandem Claisen rearrangement/intramolecular oxa-Michael addition. Beilstein Journal of Organic Chemistry. 18. 1649–1655. 2 indexed citations
12.
Bunev, Alexander S., et al.. (2022). Unusual highly diastereoselective Rh(II)-catalyzed dimerization of 3-diazo-2-arylidenesuccinimides provides access to a new dibenzazulene scaffold. Beilstein Journal of Organic Chemistry. 18. 533–538. 3 indexed citations
13.
Dar’in, Dmitry, Grigory Kantin, Alexander S. Bunev, & Mikhail Krasavin. (2022). Facile and diastereoselective arylation of the privileged 1,4-dihydroisoquinolin-3(2 H )-one scaffold. Beilstein Journal of Organic Chemistry. 18. 1070–1078. 2 indexed citations
14.
Bakulina, Olga, et al.. (2022). Dicarboxylic Acid Monoesters in β- and δ-Lactam Synthesis. Molecules. 27(8). 2469–2469. 1 indexed citations
16.
Chupakhin, Evgeny, Grigory Kantin, Dmitry Dar’in, & Mikhail Krasavin. (2021). Convenient preparation of (E)-3-arylidene-4-diazopyrrolidine-2,5-diones in array format. Mendeleev Communications. 31(1). 36–38. 12 indexed citations
17.
Kantin, Grigory, et al.. (2021). Diastereoselective Formal [5+2] Cycloaddition of Diazo Arylidene Succinimides-Derived Rhodium Carbenes and Aldehydes: A Route to 2-Benzoxepines. The Journal of Organic Chemistry. 86(19). 13673–13683. 11 indexed citations
18.
Krasavin, Mikhail, Dmitry Dar’in, Grigory Kantin, & Olga Bakulina. (2020). Facile One-Pot Access to α-Diazo-β-ketosulfones from Sulfonyl Chlorides and α-Haloketones. Synthesis. 52(15). 2259–2266. 3 indexed citations
19.
Dar’in, Dmitry, et al.. (2019). Fused vs. spiro: Kinetic, not thermodynamic preference may direct the reaction of α-carbonyl oxonium ylides. Tetrahedron Letters. 60(24). 1582–1586. 1 indexed citations
20.
Krasavin, Mikhail, Grigory Kantin, Olga Manicheva, et al.. (2017). New nitrofurans amenable by isocyanide multicomponent chemistry are active against multidrug-resistant and poly-resistant Mycobacterium tuberculosis. Bioorganic & Medicinal Chemistry. 25(6). 1867–1874. 20 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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