Alexander А. Titov

555 total citations
68 papers, 387 citations indexed

About

Alexander А. Titov is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Alexander А. Titov has authored 68 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Organic Chemistry, 16 papers in Molecular Biology and 6 papers in Pharmacology. Recurrent topics in Alexander А. Titov's work include Synthesis and pharmacology of benzodiazepine derivatives (21 papers), Synthesis and Reactivity of Heterocycles (20 papers) and Synthesis and Characterization of Pyrroles (13 papers). Alexander А. Titov is often cited by papers focused on Synthesis and pharmacology of benzodiazepine derivatives (21 papers), Synthesis and Reactivity of Heterocycles (20 papers) and Synthesis and Characterization of Pyrroles (13 papers). Alexander А. Titov collaborates with scholars based in Russia, Vietnam and Italy. Alexander А. Titov's co-authors include Leonid G. Voskressensky, А. В. Варламов, Т. Н. Борисова, Анна В. Листратова, Victor N. Khrustalev, Najoua Sbei, Л. Н. Куликова, B. Khattatov, А. В. Аксенов and Елена А. Сорокина and has published in prestigious journals such as SHILAP Revista de lepidopterología, Green Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Alexander А. Titov

57 papers receiving 379 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander А. Titov Russia 12 319 85 53 31 26 68 387
Edward J. Pack United States 11 132 0.4× 128 1.5× 33 0.6× 8 0.3× 37 1.4× 14 348
A. Papageorgiou Greece 11 93 0.3× 116 1.4× 6 0.1× 15 0.5× 149 5.7× 34 328
N. Okamura Japan 16 234 0.7× 83 1.0× 86 1.6× 15 0.5× 7 0.3× 42 562
R. W. Schumacher United States 11 97 0.3× 80 0.9× 113 2.1× 39 1.3× 23 0.9× 36 480
Kotaro Iwasaki Japan 9 338 1.1× 79 0.9× 42 0.8× 9 0.3× 14 0.5× 30 465
HIDEO TAKEDA Japan 8 177 0.6× 114 1.3× 14 0.3× 4 0.1× 25 1.0× 51 331
Hai-Tao Zhao Japan 8 79 0.2× 158 1.9× 120 2.3× 13 0.4× 14 486
Daniel J. Kerr Australia 9 363 1.1× 67 0.8× 34 0.6× 5 0.2× 3 0.1× 13 406
Günther Lahm Germany 11 275 0.9× 42 0.5× 27 0.5× 20 0.6× 2 0.1× 15 454

Countries citing papers authored by Alexander А. Titov

Since Specialization
Citations

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

Fields of papers citing papers by Alexander А. Titov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander А. Titov. 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 Alexander А. Titov. The network helps show where Alexander А. Titov may publish in the future.

Co-authorship network of co-authors of Alexander А. Titov

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander А. Titov. A scholar is included among the top collaborators of Alexander А. Titov 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 Alexander А. Titov. Alexander А. Titov 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.
Titov, Alexander А., et al.. (2025). Chemical diversity of pyrrolobenzazepine derivatives with a nodal nitrogen atom. Tetrahedron. 176. 134524–134524.
2.
Борисова, Т. Н., Артем Н. Фахрутдинов, Alexander А. Titov, et al.. (2024). Pseudo Four-Component Synthesis of 5,6-Dihydroindolo[2,1-a]isoquinolines. The Journal of Organic Chemistry. 89(2). 1045–1057. 4 indexed citations
3.
Борисова, Т. Н., et al.. (2024). Synthesis Of Dipyrrolobenzo[1,2‐a : 2′,1′‐c][1,4]diazepine Scaffold Via Three‐Component Reaction. Asian Journal of Organic Chemistry. 13(5). 1 indexed citations
4.
Titov, Alexander А., et al.. (2023). Investigation of Radiation Resistance of Heterostructure Silicon Solar Cells. Technical Physics Letters. 49(S3). S200–S203. 1 indexed citations
5.
Candia, Modesto de, Alexander А. Titov, Л. Н. Куликова, et al.. (2023). In-vitro and in-silico studies of annelated 1,4,7,8-tetrahydroazocine ester derivatives as nanomolar selective inhibitors of human butyrylcholinesterase. Chemico-Biological Interactions. 386. 110741–110741. 5 indexed citations
6.
Titov, Alexander А., Rosa Purgatorio, Анна В. Листратова, et al.. (2022). Synthesis of Isomeric 3-Benzazecines Decorated with Endocyclic Allene Moiety and Exocyclic Conjugated Double Bond and Evaluation of Their Anticholinesterase Activity. Molecules. 27(19). 6276–6276. 4 indexed citations
7.
Titov, Alexander А., Т. Н. Борисова, Leonid G. Voskressensky, et al.. (2022). Switchable light vs. acid-induced transformations of complex framework compounds at room temperature. Green Chemistry. 24(9). 3805–3813. 1 indexed citations
8.
Titov, Alexander А., Marco Catto, Modesto de Candia, et al.. (2021). Away from Flatness: Unprecedented Nitrogen-Bridged Cyclopenta[a]indene Derivatives as Novel Anti-Alzheimer Multitarget Agents. ACS Chemical Neuroscience. 12(2). 340–353. 11 indexed citations
9.
Titov, Alexander А., Rosa Purgatorio, Marco Catto, et al.. (2021). Synthesis of 8-phenyl substituted 3-benzazecines with allene moiety, their thermal rearrangement and evaluation as acetylcholinesterase inhibitors. Molecular Diversity. 26(2). 1243–1247. 4 indexed citations
10.
Борисова, Т. Н., et al.. (2021). A Three‐Component Synthesis of 3‐Functionally Substituted 5,6‐Dihydropyrrolo[2,1‐a]isoquinolines. Chemistry & Biodiversity. 19(1). e202100584–e202100584. 5 indexed citations
11.
Titov, Alexander А., et al.. (2021). Synthesis of heterocyclic systems involving [3,3]-sigmatropic rearrangements. Russian Chemical Bulletin. 70(7). 1213–1259. 17 indexed citations
12.
Titov, Alexander А., et al.. (2020). Facile Methods for the Synthesis of 8‐Ylidene‐1,2,3,8‐tetrahydrobenzazecines. European Journal of Organic Chemistry. 2020(20). 3041–3049. 8 indexed citations
14.
Titov, Alexander А., Nathaniel J. Lindsey, & Jonathan Ajo‐Franklin. (2019). Quantifying Low-Frequency DAS Response: Findings from a Laboratory Stretching Experiment. AGU Fall Meeting Abstracts. 2019. 2 indexed citations
15.
Sbei, Najoua, Анна В. Листратова, Alexander А. Titov, & Leonid G. Voskressensky. (2019). Recent Advances in Electrochemistry for the Synthesis of N-Heterocycles. Synthesis. 51(12). 2455–2473. 37 indexed citations
16.
Голованов, А. А., Т. Н. Борисова, Alexander А. Titov, et al.. (2018). Domino reactions of vinyl ethynyl ketones with 1-aryl-3,4-dihydroisoquinolines — Search for selectivity. Molecular Catalysis. 461. 67–72. 13 indexed citations
17.
Titov, Alexander А.. (2017). Measurements of Movements of Micro-Objects by the Heterodyne Method. Measurement Techniques. 60(2). 156–160. 1 indexed citations
18.
Варламов, А. В., Анна В. Листратова, Т. Н. Борисова, et al.. (2014). Transformations of 10-Substituted Tetrahydrobenzo[b][1,6]naphthyridines through Interaction with Dehydrobenzene. Chemistry of Heterocyclic Compounds. 50(2). 264–270. 4 indexed citations
19.
Voskressensky, Leonid G., et al.. (2014). Synthesis of 6-aryl-Substituted Azocino-[5,4-b]indoles from 1-aryl-Substituted 2-Ethyltetrahydro-β-Carbolines. Chemistry of Heterocyclic Compounds. 50(5). 658–669. 7 indexed citations
20.
Voskressensky, Leonid G., В. Г. Граник, Т. Н. Борисова, et al.. (2012). Synthesis of hexahydro[1,4]diazocino[7,8,1-jk]carbazoles and 1-methoxy-9-(β-vinylethylamino)ethylcarbazoles. Chemistry of Heterocyclic Compounds. 48(4). 620–624. 2 indexed citations

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