G. V. Shustov

789 total citations
47 papers, 607 citations indexed

About

G. V. Shustov is a scholar working on Organic Chemistry, Spectroscopy and Physical and Theoretical Chemistry. According to data from OpenAlex, G. V. Shustov has authored 47 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Organic Chemistry, 17 papers in Spectroscopy and 12 papers in Physical and Theoretical Chemistry. Recurrent topics in G. V. Shustov's work include Molecular spectroscopy and chirality (16 papers), Synthesis and Catalytic Reactions (15 papers) and Chemical Reaction Mechanisms (13 papers). G. V. Shustov is often cited by papers focused on Molecular spectroscopy and chirality (16 papers), Synthesis and Catalytic Reactions (15 papers) and Chemical Reaction Mechanisms (13 papers). G. V. Shustov collaborates with scholars based in Russia, Canada and Slovakia. G. V. Shustov's co-authors include Arvi Rauk, Remir G. Kostyanovsky, R. G. Kostyanovskii, Dake Yu, D. Block, David A. Armstrong, Jared M. Taylor, Г. К. Кадоркина, И. И. Червин and S. V. Varlamov and has published in prestigious journals such as Journal of the American Chemical Society, Biochemistry and The Journal of Organic Chemistry.

In The Last Decade

G. V. Shustov

43 papers receiving 574 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. V. Shustov Russia	14	397	195	168	118	105	47	607
Richard C. Reiter United States	13	394 1.0×	140 0.7×	122 0.7×	137 1.2×	125 1.2×	85	725
Carol A. Venanzi United States	13	314 0.8×	155 0.8×	250 1.5×	89 0.8×	92 0.9×	44	657
Christopher W. Doecke United States	16	479 1.2×	100 0.5×	166 1.0×	70 0.6×	89 0.8×	32	667
Andrus Metsala Estonia	12	264 0.7×	214 1.1×	133 0.8×	110 0.9×	207 2.0×	26	604
Ronald M. Jarret United States	12	381 1.0×	158 0.8×	140 0.8×	118 1.0×	84 0.8×	28	573
Yujiro Nomura Japan	13	465 1.2×	119 0.6×	105 0.6×	53 0.4×	65 0.6×	76	626
Fernando Sancassan Italy	17	481 1.2×	205 1.1×	101 0.6×	89 0.8×	44 0.4×	71	644
Giovanni Cerioni Italy	16	454 1.1×	175 0.9×	59 0.4×	117 1.0×	57 0.5×	54	631
A. L. BAUMSTARK United States	15	639 1.6×	207 1.1×	120 0.7×	78 0.7×	54 0.5×	63	851
M.T. Tribble United States	9	413 1.0×	237 1.2×	84 0.5×	172 1.5×	117 1.1×	13	710

Countries citing papers authored by G. V. Shustov

Since Specialization

Citations

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

Fields of papers citing papers by G. V. Shustov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. V. Shustov. 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 G. V. Shustov. The network helps show where G. V. Shustov may publish in the future.

Co-authorship network of co-authors of G. V. Shustov

This figure shows the co-authorship network connecting the top 25 collaborators of G. V. Shustov. A scholar is included among the top collaborators of G. V. Shustov 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 G. V. Shustov. G. V. Shustov 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

Kostyanovsky, Remir G., et al.. (1998). Sterically controlled population of the 1,2-cis-form of 1,2-dimethyl-3-tert-butyldiaziridine. Mendeleev Communications. 8(3). 113–115. 8 indexed citations

Shustov, G. V., et al.. (1995). A Novel trans-1,2-Dimethyldiaziridine–Silver Nitrate Complex: Synthesis and Molecular and Crystal Structure. Mendeleev Communications. 5(6). 218–219. 5 indexed citations

Shustov, G. V. & Arvi Rauk. (1995). Conformational and Chiroptical Properties of N-Nitrosoazetidines. Journal of the American Chemical Society. 117(3). 928–934. 19 indexed citations

Rauk, Arvi, et al.. (1994). The vibrational circular dichroism spectra of 2-methylaziridine: dominance of the asymmetric centre at nitrogen. Canadian Journal of Chemistry. 72(3). 506–513. 6 indexed citations

Shustov, G. V., et al.. (1994). Stereochemistry and chiroptical properties of 1,3-dialkylaziridinones (α-lactams). Chiral rules for the nonplanar amide chromophore. Canadian Journal of Chemistry. 72(2). 279–286. 8 indexed citations

Wieser, Hal, et al.. (1993). Local and framework stereochemical markers in vibrational circular dichroism: 1,2- and 2,3-dimethylaziridines. Canadian Journal of Chemistry. 71(12). 2028–2037. 5 indexed citations

Shustov, G. V., et al.. (1992). Stereochemistry and chiroptical properties of the nonplanar nitrosamine group in N-nitrosoaziridines. Journal of the American Chemical Society. 114(21). 8257–8262. 14 indexed citations

Shustov, G. V., et al.. (1992). Chiroptical properties of the non-planar nitrosamine chromophore in N-nitrosaziridines. Journal of the Chemical Society Chemical Communications. 705–705. 3 indexed citations

Shustov, G. V., et al.. (1992). Asymmetric nitrogen. 76. Quantum chemical study of geometry and configurational stability of ketenimines. Russian Chemical Bulletin. 41(11). 2028–2033. 2 indexed citations

10.

Shustov, G. V., et al.. (1992). The nonplanar amide group in N-acylaziridines: conformational behavior and chiroptical properties. Journal of the American Chemical Society. 114(5). 1616–1623. 59 indexed citations

11.

Shustov, G. V., S. V. Varlamov, Arvi Rauk, & R. G. Kostyanovskii. (1990). Chiroptical properties of the diazirine chromophore. Journal of the American Chemical Society. 112(9). 3403–3408. 15 indexed citations

12.

Shustov, G. V., et al.. (1988). Asymmetric nitrogen 61. Inversion topomerization of diaziridines. Russian Chemical Bulletin. 37(8). 1671–1677. 2 indexed citations

13.

Shustov, G. V., Sergey N. Denisenko, Michael Shokhen, & R. G. Kostyanovskii. (1988). Asymmetric nitrogen 60. Acylation as a pathway to optically active 1,3,3-trisubstituted diaziridines. Russian Chemical Bulletin. 37(8). 1665–1671. 6 indexed citations

14.

Shustov, G. V., Sergey N. Denisenko, И. И. Червин, & R. G. Kostyanovskii. (1988). Fluorodeoxygenation of proline, optically active 2-trifluoromethylpyrrolidine, and its chromophoric derivatives. Russian Chemical Bulletin. 37(7). 1422–1427. 2 indexed citations

15.

Shustov, G. V., Sergey N. Denisenko, И. И. Червин, N. L. Asfandiarov, & Remir G. Kostyanovsky. (1985). Asymmetric nitrogen—41. Tetrahedron. 41(23). 5719–5731. 43 indexed citations

16.

Zaichenko, N. L., et al.. (1984). Asymmetrical nitrogen. Communication 34. Steric selectivity of the methylenation of activated O-alkyloximes. Russian Chemical Bulletin. 33(3). 546–557. 1 indexed citations

17.

Shustov, G. V., Sergey N. Denisenko, & R. G. Kostyanovskii. (1983). Stable N-chlorodiaziridines. Russian Chemical Bulletin. 32(8). 1754–1755.

18.

Shustov, G. V., et al.. (1982). Oxidative cleavage of vicinal bis(hydroxylamines). Russian Chemical Bulletin. 31(2). 330–339. 3 indexed citations

19.

Shustov, G. V., et al.. (1981). Derivatives of diazirine-3,3-dicarboxylic acid. Chemistry of Heterocyclic Compounds. 17(7). 662–667. 1 indexed citations

20.

Kostyanovskii, R. G., G. V. Shustov, & Victor I. Markov. (1974). Diaziridine-3,3-dicarboxylic acid derivatives. Russian Chemical Bulletin. 23(12). 2725–2728. 1 indexed citations

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