Т. Н. Борисова

1.2k citations

125 papers · 844 indexed · h-index 16

Organic Chemistry top 2%
Molecular Biology
Pharmacology top 10%
Cancer Research
Computational Theory and Mathematics top 10%

Co-authors: А. В. Варламов Leonid G. Voskressensky Л. Н. Куликова Анна В. Листратова Alexander А. Titov Cosimo Altomare Victor N. Khrustalev Marco Catto
Topics: Synthesis and Reactivity of Heterocycles (53 papers)Synthesis and pharmacology of benzodiazepine derivatives (50 papers)Synthesis and Characterization of Pyrroles (26 papers)
Cited by: Organic Chemistry Pharmacology Toxicology
Journals: SHILAP Revista de lepidopterologíaGreen Chemistry The Journal of Organic Chemistry
Partner nations: Russia Italy Ukraine

In The Last Decade

Т. Н. Борисова

109 papers receiving 839 citations

Peers

Countries citing papers authored by Т. Н. Борисова

Since Specialization

Citations

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

Fields of papers citing papers by Т. Н. Борисова

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Т. Н. Борисова. 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 Т. Н. Борисова. The network helps show where Т. Н. Борисова may publish in the future.

Co-authorship network of co-authors of Т. Н. Борисова

This figure shows the co-authorship network connecting the top 25 collaborators of Т. Н. Борисова. A scholar is included among the top collaborators of Т. Н. Борисова 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 Т. Н. Борисова. Т. Н. Борисова 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

#	Work	Indexed citations
1	Pseudo Four-Component Synthesis of 5,6-Dihydroindolo[2,1-a]isoquinolines 2024 ·The Journal of Organic Chemistry ·(unknown),Т. Н. Борисова,Артем Н. Фахрутдинов,(unknown),Alexander А. Titov,(unknown),В. А. Тафеенко,А. В. Варламов,Leonid G. Voskressensky	4
2	Nature-Inspired 1-Phenylpyrrolo[2,1-a]isoquinoline Scaffold for Novel Antiproliferative Agents Circumventing P-Glycoprotein-Dependent Multidrug Resistance 2024 ·Pharmaceuticals ·(unknown),Rosa Purgatorio,Т. Н. Борисова,А. В. Варламов,Л. В. Аникина,(unknown),(unknown),Mauro Niso,Nicola Antonio Colabufo,Antonio Carrieri,Marco Catto,Modesto de Candia,Leonid G. Voskressensky,Cosimo Altomare	0
3	Synthesis Of Dipyrrolobenzo[1,2‐a : 2′,1′‐c][1,4]diazepine Scaffold Via Three‐Component Reaction 2024 ·Asian Journal of Organic Chemistry ·(unknown),Т. Н. Борисова,(unknown),(unknown),(unknown),Антон А. Шетнев,Alexander А. Titov,А. В. Варламов,Leonid G. Voskressensky	1
4	Three-Component Synthesis of New C3-Substituted 5,6-Dihydropyrrolo[2,1-a]isoquinolines 2023 ·Russian Journal of Organic Chemistry ·(unknown),(unknown),Т. Н. Борисова,Артем Н. Фахрутдинов,Alexander А. Titov,Елена А. Сорокина,А. В. Варламов	1
5	Switchable light vs. acid-induced transformations of complex framework compounds at room temperature 2022 ·Green Chemistry ·(unknown),Alexander А. Titov,Т. Н. Борисова,Leonid G. Voskressensky,А. В. Варламов,Massimo Christian D’Alterio,Alessio Petrone,Rafael Luque,Giovanni Talarico	1
6	Synthesis of Isomeric 3-Benzazecines Decorated with Endocyclic Allene Moiety and Exocyclic Conjugated Double Bond and Evaluation of Their Anticholinesterase Activity 2022 ·Molecules ·Alexander А. Titov,Rosa Purgatorio,(unknown),Анна В. Листратова,Т. Н. Борисова,Modesto de Candia,Marco Catto,Cosimo Altomare,А. В. Варламов,Leonid G. Voskressensky	4
7	Away from Flatness: Unprecedented Nitrogen-Bridged Cyclopenta[a]indene Derivatives as Novel Anti-Alzheimer Multitarget Agents 2021 ·ACS Chemical Neuroscience ·Alexander А. Titov,(unknown),Marco Catto,Modesto de Candia,Nicola Gambacorta,Nunzio Denora,Leonardo Pisani,Orazio Nicolotti,Т. Н. Борисова,А. В. Варламов,Leonid G. Voskressensky,Cosimo Altomare	11
8	A Three‐Component Synthesis of 3‐Functionally Substituted 5,6‐Dihydropyrrolo[2,1‐a]isoquinolines 2021 ·Chemistry & Biodiversity ·(unknown),Т. Н. Борисова,Alexander А. Titov,(unknown),Роман А. Новиков,(unknown),А. В. Варламов,Leonid G. Voskressensky	5
9	Homobivalent Lamellarin-Like Schiff Bases: In Vitro Evaluation of Their Cancer Cell Cytotoxicity and Multitargeting Anti-Alzheimer’s Disease Potential 2021 ·Molecules ·(unknown),Л. В. Аникина,Rosa Purgatorio,Marco Catto,Orazio Nicolotti,Modesto de Candia,Leonardo Pisani,Т. Н. Борисова,(unknown),А. В. Варламов,(unknown),Р. С. Борисов,Leonid G. Voskressensky,Cosimo Altomare	10
10	Synthesis of 8-phenyl substituted 3-benzazecines with allene moiety, their thermal rearrangement and evaluation as acetylcholinesterase inhibitors 2021 ·Molecular Diversity ·(unknown),Alexander А. Titov,(unknown),Rosa Purgatorio,Marco Catto,Елена А. Сорокина,Т. Н. Борисова,А. В. Варламов,Cosimo Altomare,Leonid G. Voskressensky	4
11	Facile synthesis of pyrrolo[2,1-a]isoquinolines by domino reaction of 1-aroyl-3,4-dihydroisoquinolines with conjugated ketones, nitroalkenes and nitriles 2020 ·Molecular Diversity ·(unknown),(unknown),Т. Н. Борисова,(unknown),Alexander А. Titov,А. В. Варламов,Leonid G. Voskressensky,(unknown)	3
12	Transformations of tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidin-4(3H)-ones in the presence of alkynes bearing electron-withdrawing substituents 2012 ·Russian Chemical Bulletin ·Leonid G. Voskressensky,Т. Н. Борисова,(unknown),Анна В. Листратова,Л. Н. Куликова,Victor N. Khrustalev,(unknown),А. В. Варламов	6
13	The reaction of tetrahydrochromeno[3,4-c]pyridines with activated alkynes. The first synthesis of tetrahydrochromeno[4,3-d]azocines 2011 ·Tetrahedron Letters ·Leonid G. Voskressensky,Л. Н. Куликова,(unknown),Victor N. Khrustalev,Т. Н. Борисова,Анна В. Листратова,(unknown),А. В. Варламов	9
14	Transformations of tetrahydro-pyrido[4,3-d]pyrimidines [b]-condensed with isoxazole, thiazole, thiadiazole, and triazole units under the action of activated alkynes 2008 ·Chemistry of Heterocyclic Compounds ·Leonid G. Voskressensky,Т. Н. Борисова,(unknown),Л. Н. Куликова,Елена А. Сорокина,Р. С. Борисов,А. В. Варламов	8
15	Ester derivatives of annulated tetrahydroazocines: A new class of selective acetylcholinesterase inhibitors 2006 ·Bioorganic & Medicinal Chemistry ·Andrea Carotti,Modesto de Candia,Marco Catto,Т. Н. Борисова,А. В. Варламов,Estefanı́a Méndez-Álvarez,Ramón Soto‐Otero,Leonid G. Voskressensky,Cosimo Altomare	28
16	Tandem Cleavage of Hydrogenated β‐ and γ‐Carbolines − New Practical Synthesis of Tetrahydroazocino[4,5‐b]indoles and Tetrahydroazocino[5,4‐b]indoles Showing Acetylcholinesterase Inhibitory Activity 2004 ·European Journal of Organic Chemistry ·Leonid G. Voskressensky,Т. Н. Борисова,Л. Н. Куликова,А. В. Варламов,Marco Catto,Cosimo Altomare,Angelo Carotti	56
17	TANDEM MICHAEL ADDITION - HOFFMAN ELIMINATION SEQUENCE OF DMAD ON TETRAHYDROPYRROLO[3,2-C]PYRIDINES. NEW ROUTE TO VINYLPYRROLES . 2001 ·Heterocyclic Communications ·А. В. Варламов,Т. Н. Борисова,Leonid G. Voskressensky,(unknown),(unknown)	14
18	Unusual Reaction of 4,5,7-Trimethyl-1-vinyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridine with Tetracyanoethylene 2001 ·Chemistry of Heterocyclic Compounds ·А. В. Варламов,Т. Н. Борисова,(unknown),Г.Г. Александров,Leonid G. Voskressensky,(unknown)	0
19	Pyrrolo[3,2-c]pyridine derivatives as inhibitors of platelet aggregation 2000 ·Bioorganic & Medicinal Chemistry Letters ·Cosimo Altomare,Luciana Summo,Saverio Cellamare,А. В. Варламов,Leonid G. Voskressensky,Т. Н. Борисова,Angelo Carotti	16
20	Unusual transformations of 1-vinyl-4,5,6,7-tetrahydro-5-methyl-4,6-ethanopyrrolo[3,2-c]pyridine to cyclohepteno[b]pyrroles under acetylation conditions 2000 ·ARKIVOC ·А. В. Варламов,Т. Н. Борисова,Leonid G. Voskressensky,(unknown),(unknown)	1

About Т. Н. Борисова

Т. Н. Борисова is a scholar working on Organic Chemistry, Pharmacology and Cancer Research, having authored 125 papers that have together received 844 indexed citations. Recurring topics across this work include Synthesis and Reactivity of Heterocycles (53 papers), Synthesis and pharmacology of benzodiazepine derivatives (50 papers) and Synthesis and Characterization of Pyrroles (26 papers). The work is most often cited by research in Organic Chemistry (786 citations), Pharmacology (154 citations) and Toxicology (19 citations). Т. Н. Борисова has collaborated with scholars based in Russia, Italy and Ukraine. Frequent co-authors include А. В. Варламов, Leonid G. Voskressensky, Л. Н. Куликова, Анна В. Листратова, Alexander А. Titov, Cosimo Altomare, Victor N. Khrustalev, Marco Catto, Р. С. Борисов and Angelo Carotti. Their work appears in journals such as SHILAP Revista de lepidopterología, Green Chemistry and The Journal of Organic Chemistry.

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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