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Статьи (147)

# Публикация
1 Kudryavtseva E.N. , Zholtovskaya A.A. , Lichitsky B.V.
Synthesis of Substituted Pyrrolo[2,3‐ c ]Pyrazol‐4‐Ylacetic Acids via Acid‐Catalyzed Rearrangement of Aroyl‐Containing Pyrazolo[3,4‐ b ]Pyridin‐6‐Ones
Journal of Heterocyclic Chemistry. 2026. DOI: 10.1002/jhet.70182 Scopus OpenAlex
2 Lichitsky B.V. , Kudryavtseva T.A. , Kudryavtseva E.N.
Straightforward synthesis of imidazo[4,5-b]indeno[2,1-e]pyridin-9(3H)-one framework via multicomponent reaction of 5-aminoimidazoles with aldehydes and 1,3-indandione
Tetrahedron. 2026. V.190. 135064 . DOI: 10.1016/j.tet.2025.135064 WOS Scopus OpenAlex
3 Theodosis-Nobelos P. , Papagiouvannis G. , Fesatidou M. , Marc G. , Geronikaki A. , Lichitsky B. , Kartsev V. , Komogortsev A. , Sirakanyan S.
Design and Synthesis of Fused Derivatives of 7-Hydroxycoumarin (Umbelliferone) with the Flavonol Quercetin and the Flavone Luteolin-Analysis of Their Antioxidant and Physicochemical Properties
Oxygen. 2026. V.6. N1. 3 . DOI: 10.3390/oxygen6010003 OpenAlex
4 Petrou A. , Deruvo C. , Purgatorio R. , Lichitsky B. , Komogortsev A.N. , Kartsev V.G. , de Candia M. , Catto M. , Altomare C.D. , Geronikaki A.
Investigating Amphoteric 3,4′-Biscoumarin-Based ortho-[(Dialkylamino)methyl]phenols as Dual MAO and ChE Inhibitors
International Journal of Molecular Sciences. 2025. V.26. N20. 10197 . DOI: 10.3390/ijms262010197 WOS Scopus OpenAlex
5 Milyutin C.V. , Lichitsky B.V. , Komogortsev A.N.
Structurally Dependent Acid‐Catalyzed Cyclization of (het)arylbisallomaltol Derivatives
Journal of Heterocyclic Chemistry. 2025. V.62. N11. P.1409-1423. DOI: 10.1002/jhet.70085 WOS Scopus OpenAlex
6 Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V.
Study of the interaction of 2H-furo[3,2-b]pyran-2-ones with nitrogen-containing nucleophiles
Beilstein Journal of Organic Chemistry. 2025. V.21. P.556-563. DOI: 10.3762/bjoc.21.44 WOS Scopus OpenAlex
7 Kudryavtseva T.A. , Kudryavtseva E.N. , Lichitsky B.V.
Synthesis of 9H‐Indeno[1,2‐b]Thieno[2,3‐e]Pyridin‐9‐One System Based on Multicomponent Reaction of 3‐Aminothiophenes With Aldehydes and 1,3‐Indandione
Journal of Heterocyclic Chemistry. 2025. V.62. N12. P.1916-1927. DOI: 10.1002/jhet.70107 WOS Scopus OpenAlex
8 Kudryavtseva E. , Lichitsky B. , Tretyakov E.
A Multi‐component Reaction of Hexafluoro‐1,4‐naphthoquinone with N‐Heterocycles and Active Methylene Compounds: A Straightforward Approach to Polyfluorinated Zwitterions
Asian Journal of Organic Chemistry. 2025. V.14. N4. e202400751 . DOI: 10.1002/ajoc.202400751 WOS Scopus OpenAlex
9 Migulin A.V. , Milyutin C.V. , Lichitsky B.V. , Korobkov S.M. , Komogortsev A.N.
Investigation of the photochemical behavior of allomaltol-containing 2-aminothiazole derivatives
Organic & Biomolecular Chemistry. 2025. V.23. P.4172-4185. DOI: 10.1039/d5ob00264h WOS Scopus OpenAlex
10 Kudryavtseva E.N. , Lichitsky B.V. , Tretyakov E.V.
A reaction of hexafluoro-1,4-naphthoquinone with 2-aminopyridines
Mendeleev Communications. 2025. V.35. N3. P.258-260. DOI: 10.71267/mencom.7737 WOS Scopus OpenAlex
11 Bakuleva N.A. , Lichitskii B.V. , Komogortsev A.N. , Tretyakov E.V.
Construction of a 1,2-diazetidine core based on a multicomponent reaction of N,N′-(2,3-dimethylbutane-2,3-diyl)bis(hydroxylamine), arylglyoxals, and Meldrum's acid
Organic & Biomolecular Chemistry. 2025. V.23. P.4997-5005. DOI: 10.1039/d5ob00545k WOS Scopus OpenAlex
12 Bakuleva N.A. , Lichitskii B.V. , Samigullina A.I. , Tretyakov E.V.
Synthesis, Molecular and Crystal Structures of 4-Oxo-1,2-Dihydro-4H-Pyrrolo[3,2,1-ij]Quinolin-5-yl)-Substituted Nitronylnitroxyl
Journal of Structural Chemistry. 2025. V.66. N8. P.1606-1612. DOI: 10.1134/s0022476625080086 WOS Scopus OpenAlex
13 Komogortsev A.N. , Milyutin C.V. , Lichitsky B.V. , Migulin V.A.
UV-assisted rearrangement of substituted 3-arylaminopyrazoles with an allomaltol fragment into tricyclic cyclopenta[4,5]pyrrolo[2,3-c]pyrazole derivatives
Organic & Biomolecular Chemistry. 2025. V.23. N28. P.6738-6744. DOI: 10.1039/d5ob00796h WOS Scopus OpenAlex
14 Bakuleva N.A. , Lichitskii B.V. , Komogortsev A.N. , Tretyakov E.V.
The study of the photochemical behavior of 5-aryl-2,3-dihydropyrazine 1,4-dioxides
Organic & Biomolecular Chemistry. 2025. V.23. P.369-376. DOI: 10.1039/d4ob01570c WOS Scopus OpenAlex
15 Todsaporn D. , Sanachai K. , Aonbangkhen C. , Geronikaki A. , Kartsev V. , Lichitsky B. , Komogortsev A. , Maitarad P. , Rungrotmongkol T.
Exploring Novel Furochochicine Derivatives as Promising JAK2 Inhibitors in HeLa cells: Integrating Docking, QSAR-ML, MD Simulations, and Experiments
Computational and Structural Biotechnology Journal. 2025. V.27. P.3625-3639. DOI: 10.1016/j.csbj.2025.08.007 WOS Scopus OpenAlex
16 Kudryavtseva T.A. , Kudryavtseva E.N. , Lichitsky B.V.
Synthesis of Substituted Dithiazolo[4,5‐b:5′,4′‐e] Pyridine‐2,6‐Diamines Based on the Interaction of 2,4‐Diaminothiazole With Aldehydes
Journal of Heterocyclic Chemistry. 2025. V.62. N10. P.1218-1227. DOI: 10.1002/jhet.70039 WOS Scopus OpenAlex
17 Kudryavtseva E.N. , Lichitsky B.V. , Tretyakov E.V.
Investigation of the reaction of hexafluoro-1,4-naphthoquinone with substituted phenols
Journal of Fluorine Chemistry. 2025. V.282. 110402 . DOI: 10.1016/j.jfluchem.2025.110402 WOS Scopus OpenAlex
18 Kudryavtseva E.N. , Lichitsky B.V. , Komogortsev A.N. , Milyutin C.V. , Tretyakov E.V.
The Study of Reaction of Hexafluoro‐1,4‐Napthoquinone With Substituted 5‐Aminopyrazoles
Journal of Heterocyclic Chemistry. 2024. V.61. N12. P.1932-1941. DOI: 10.1002/jhet.4911 WOS Scopus OpenAlex
19 Kudryavtseva E.N. , Lichitsky B.V. , Komogortsev A.N. , Milyutin C.V. , Tretyakov E.V.
Synthesis of substituted 5,6,7,8‐tetrafluoro‐1H‐benzo[f]indol‐4,9‐diones based on the reaction of hexafluoro‐1,4‐napthoquinone with methyl 3‐aminocrotonates
Journal of Heterocyclic Chemistry. 2024. V.61. N10. P.1554-1563. DOI: 10.1002/jhet.4872 WOS Scopus OpenAlex
20 Kudryavtseva E.N. , Lichitsky B.V. , Tretyakov E.V.
Synthesis of Substituted N'‐(3,5,6,7,8‐Pentafluoro‐1,4‐Dioxo‐1,4‐Dihydronaphthalen‐2‐yl)Hydrazides by Condensation of Acyl Hydrazines and Perfluoro‐1,4‐Naphthoquinone
ChemistrySelect. 2024. V.9. N43. e202404996 . DOI: 10.1002/slct.202404996 WOS Scopus OpenAlex

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