М. К. Грачев

479 total citations
75 papers, 325 citations indexed

About

М. К. Грачев is a scholar working on Pharmaceutical Science, Spectroscopy and Organic Chemistry. According to data from OpenAlex, М. К. Грачев has authored 75 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Pharmaceutical Science, 34 papers in Spectroscopy and 32 papers in Organic Chemistry. Recurrent topics in М. К. Грачев's work include Drug Solubulity and Delivery Systems (49 papers), Analytical Chemistry and Chromatography (31 papers) and Crystallization and Solubility Studies (22 papers). М. К. Грачев is often cited by papers focused on Drug Solubulity and Delivery Systems (49 papers), Analytical Chemistry and Chromatography (31 papers) and Crystallization and Solubility Studies (22 papers). М. К. Грачев collaborates with scholars based in Russia and China. М. К. Грачев's co-authors include Э. Е. Нифантьев, L. K. Vasyanina, Ирина И. Левина, E. E. NIFANT'EV, А. А. Степанов, L. O. Kononov, В. А. Гринберг, Alexey M. Yashchenok, Maria V. Lomova and Dmitry A. Gorin and has published in prestigious journals such as Chemical Reviews, Russian Chemical Reviews and Journal of Inclusion Phenomena and Macrocyclic Chemistry.

In The Last Decade

М. К. Грачев

67 papers receiving 306 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
М. К. Грачев Russia 8 183 169 107 106 74 75 325
Alexander G. Kirilenko Russia 8 337 1.8× 249 1.5× 53 0.5× 262 2.5× 38 0.5× 9 472
E. E. NIFANT'EV Russia 9 221 1.2× 36 0.2× 34 0.3× 43 0.4× 61 0.8× 87 316
Екатерина Е. Галенко Russia 15 566 3.1× 60 0.4× 21 0.2× 85 0.8× 66 0.9× 51 635
Greg Butler China 8 263 1.4× 192 1.1× 11 0.1× 52 0.5× 22 0.3× 12 381
日本化学会 3 325 1.8× 306 1.8× 13 0.1× 77 0.7× 23 0.3× 8 455
Harbans S. Sachdev United States 11 250 1.4× 24 0.1× 32 0.3× 121 1.1× 22 0.3× 27 371
Alena Budinská Switzerland 10 256 1.4× 131 0.8× 24 0.2× 70 0.7× 60 0.8× 15 380
Tarun K. Maishal France 10 222 1.2× 16 0.1× 27 0.3× 45 0.4× 86 1.2× 13 330
Jun‐Chen Kang China 10 363 2.0× 48 0.3× 24 0.2× 30 0.3× 33 0.4× 15 431
Joby Winn United Kingdom 8 313 1.7× 9 0.1× 72 0.7× 94 0.9× 114 1.5× 9 365

Countries citing papers authored by М. К. Грачев

Since Specialization
Citations

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

Fields of papers citing papers by М. К. Грачев

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of М. К. Грачев

This figure shows the co-authorship network connecting the top 25 collaborators of М. К. Грачев. A scholar is included among the top collaborators of М. К. Грачев 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. К. Грачев. М. К. Грачев 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.
Грачев, М. К., et al.. (2019). Phosphorylation of 1,4:3,6-Dianhydro-d-sorbitol. Russian Journal of General Chemistry. 89(5). 939–943. 1 indexed citations
2.
Грачев, М. К., et al.. (2019). Cationic β-cyclodextrin derivatives containing 2-(4-isobutylphenyl)- and 2-(3-benzoylphenyl)propionic acid residues. Russian Chemical Bulletin. 68(4). 862–866. 2 indexed citations
3.
Vasyanina, L. K., et al.. (2015). Direct esterification of the hydroxyl groups of β-cyclodextrin with some aromatic monocarboxylic acids. Russian Journal of General Chemistry. 85(11). 2605–2608. 4 indexed citations
4.
Левина, Ирина И., et al.. (2015). Esterification of 2-hydroxypropyl β-cyclodextrin derivative with some aromatic monocarboxylic acids. Russian Journal of Organic Chemistry. 51(10). 1395–1397. 2 indexed citations
5.
Грачев, М. К., et al.. (2014). Acylation of per-6-O-(tert-butyl)(dimethyl)silyl-α-cyclodextrin with acetylsalicylic chloride. Russian Journal of General Chemistry. 84(8). 1646–1647. 3 indexed citations
6.
Грачев, М. К., et al.. (2014). Nanoscaled inclusion complexes of β-cyclodextrin with binuclear compounds based on diols containing fragments of selected aromatic monocarboxylic acids. Russian Journal of General Chemistry. 84(4). 753–757. 3 indexed citations
7.
Грачев, М. К., et al.. (2013). Amphiphilic conjugates of β-cyclodextrin with acetylsalicylic and 2-(4-isobutylphenyl)propionic acids. Russian Journal of Organic Chemistry. 49(12). 1777–1782. 3 indexed citations
8.
Грачев, М. К., et al.. (2013). Bromination of deactivated polycyclic aromatic nitro compounds. Russian Journal of Organic Chemistry. 49(10). 1474–1481. 2 indexed citations
9.
Грачев, М. К., et al.. (2011). Biological Activity of Some Derivatives of β-Cyclodextrin. Bulletin of Experimental Biology and Medicine. 151(6). 698–701. 1 indexed citations
10.
Грачев, М. К., et al.. (2011). Acetylation of α- and β-cyclodextrines. Russian Journal of Organic Chemistry. 47(2). 284–289. 10 indexed citations
11.
Грачев, М. К., et al.. (2011). α-Cyclodextrin compounds containing benzoic, acetylsalicylic, and 2-(4-isobutylphenyl)propionic acid residues. Russian Journal of Organic Chemistry. 47(7). 981–988. 7 indexed citations
12.
Грачев, М. К., et al.. (2010). Cyclophosphorylation of β-cyclodextrin silyl derivatives with trivalent phosphorus acids dichlorides. Russian Journal of General Chemistry. 80(10). 1933–1936. 4 indexed citations
13.
Грачев, М. К., et al.. (2008). Competitive phosphorylation of some β-cyclodextrin-based inclusion compounds with phosphorous diamidoester. Russian Journal of General Chemistry. 78(1). 57–60. 1 indexed citations
14.
Грачев, М. К., et al.. (2004). Peculiarities of the Chemical Behavior of a Per-P(III)-Derivative of β-Cyclodextrin. Russian Journal of General Chemistry. 74(5). 808–809. 4 indexed citations
15.
Грачев, М. К., et al.. (2004). Inclusion compounds of some water-soluble β-cyclodextrin derivatives with phenolphthalein. Russian Journal of General Chemistry. 74(12). 1922–1925. 7 indexed citations
16.
Грачев, М. К., et al.. (2003). Monophosphorylation of 1,4:3,6-dianhydro-D-mannitol. Russian Chemical Bulletin. 52(4). 1009–1012. 1 indexed citations
17.
Грачев, М. К., et al.. (2003). Synthesis of Phosphocapped Derivatives of β-Cyclodextrin. Russian Journal of General Chemistry. 73(12). 1945–1946. 3 indexed citations
18.
Грачев, М. К., et al.. (2001). Cyclophosphorylation of tert-Butyldimethylsilyl Derivatives of Cyclodextrins. Russian Journal of General Chemistry. 71(6). 884–887. 2 indexed citations
19.
Грачев, М. К., et al.. (2000). Amides of Trivalent Phosphorus Acids as Phosphorylating Reagents for Proton-Donating Nucleophiles. Chemical Reviews. 100(10). 3755–3800. 85 indexed citations
20.
Грачев, М. К., et al.. (1994). Trivalent phosphorus acids amides as phosphorylating agents for alcohols and amines. Russian Chemical Reviews. 63(7). 575–609. 15 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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