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Articles (147) More info

1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
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	Komogortsev A.N. , Lichitsky B.V. , Milyutin C.V. , Melekhina V.G. Straightforward method for the synthesis of 2H‐furo[3,2‐b]pyran‐2‐one derivatives starting from allomaltol Journal of Heterocyclic Chemistry. 2024. V.61. N1. P.86-92. DOI: 10.1002/jhet.4744 WOS Scopus OpenAlex
19	Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V. , Melekhina V.G. Synthesis of allomaltol containing terarylenes with imidazole N -oxides bridge fragment Synthetic Communications. 2024. V.54. N6. P.460-470. DOI: 10.1080/00397911.2024.2310522 WOS Scopus OpenAlex
20	Tsyganov D.V. , Lichitsky B.V. , Melekhina V.G. , Komogortsev A.N. Facile Synthesis of Furo[3,2- b ]Chromen-3-Ylacetic Acids via Multicomponent Reaction of 3-Hydroxy-4 H -Chromen-4-Ones, Arylglyoxals, and Meldrum’s Acid Polycyclic Aromatic Compounds. 2024. V.44. N7. P.4885-4894. DOI: 10.1080/10406638.2023.2258255 WOS Scopus OpenAlex
21	Komogortsev A.N. , Melekhina V. , Lichitskii B. Anionic photochemical rearrangement of 3-hydroxypyran-4-ones bearing oxazol-2-one fragment Organic & Biomolecular Chemistry. 2024. V.22. N8. P.1686-1692. DOI: 10.1039/d3ob01957h WOS Scopus OpenAlex
22	Bakuleva N.A. , Lichitsky B.V. , Tsyganov D.V. , Komogortsev A.N. , Melekhina V.G. , Tretyakov E.V. Synthesis of substituted 5‐aryl‐2,3‐dihydropyrazine 1,4‐dioxides based on condensation of N,N′‐(2,3‐dimethylbutane‐2,3‐diyl)bis(hydroxylamine) with various arylglyoxals Journal of Heterocyclic Chemistry. 2024. V.61. N7. P.1057-1065. DOI: 10.1002/jhet.4826 WOS Scopus OpenAlex
23	Tsyganov D.V. , Komogortsev A.N. , Melekhina V.G. , Fakhrutdinov A.N. , Lichitsky B.V. Photochemical method for preparation of benzo[a]pyrano[3,2‐c]phenazin‐4‐ones from quinoxalines with 4‐pyranone unit Journal of Heterocyclic Chemistry. 2024. V.61. N9. P.1387-1398. DOI: 10.1002/jhet.4861 WOS Scopus OpenAlex
24	Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V. Synthesis of 1,2,3-triazoles containing an allomaltol moiety from substituted pyrano[2,3-d]isoxazolones via base-promoted Boulton–Katritzky rearrangement Beilstein Journal of Organic Chemistry. 2024. V.20. P.1334-1340. DOI: 10.3762/bjoc.20.117 WOS Scopus OpenAlex
25	Komogortsev A.N. , Melekhina V.G. , Milyutin C.V. , Lichitsky B.V. Synthesis of 2‐aminothiazoles containing 3‐hydroxypyran‐4‐one fragment based on condensation of substituted α‐arylaminoketones with thiourea Journal of Heterocyclic Chemistry. 2024. V.61. N10. P.1531-1541. DOI: 10.1002/jhet.4876 WOS Scopus OpenAlex
26	Komogortsev A.N. , Milyutin C.V. , Lichitsky B.V. Base-promoted cascade recyclization of allomaltol derivatives containing an amide fragment into substituted 3-(1-hydroxyethylidene)tetronic acids Beilstein Journal of Organic Chemistry. 2024. V.20. P.2585-2591. DOI: 10.3762/bjoc.20.217 WOS Scopus OpenAlex
27	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
28	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
29	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
30	Egorov M.P. , Ananikov V.P. , Baskir E.G. , Boganov S.E. , Bogdan V.I. , Vereshchagin A.N. , Vil’ V.A. , Dalinger I.L. , Dilman A.D. , Eliseev O.L. , Zlotin S.G. , Knyazeva E.A. , Kogan V.M. , Kononov L.O. , Krayushkin M.M. , Krylov V.B. , Kustov L.M. , Levin V.V. , Lichitsky B.V. , Medvedev M.G. , Nifantiev N.E. , Rakitin O.A. , Sakharov A.M. , Svitanko I.V. , Smirnov G.A. , Stakheev A.Y. , Syroeshkin M.A. , Terent’ev A.O. , Tomilov Y.V. , Tretyakov E.V. , Trushkov I.V. , Fershtat L.L. , Chaliy V.A. , Shirinian V.Z. Current trends in organic chemistry: contribution of the N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences Russian Chemical Bulletin. 2024. V.73. N9. P.2423-2532. DOI: 10.1007/s11172-024-4366-8 WOS Scopus OpenAlex
31	Angeli A. , Petrou A. , Kartsev V. , Lichitsky B. , Komogortsev A. , Capasso C. , Geronikaki A. , Supuran C.T. Synthesis, Biological and In Silico Studies of Griseofulvin and Usnic Acid Sulfonamide Derivatives as Fungal, Bacterial and Human Carbonic Anhydrase Inhibitors International Journal of Molecular Sciences. 2023. V.24. N3. 2802 . DOI: 10.3390/ijms24032802 WOS Scopus OpenAlex
32	Angeli A. , Kartsev V. , Petrou A. , Lichitsky B. , Komogortsev A. , Geronikaki A. , Supuran C.T. Substituted furan sulfonamides as carbonic anhydrase inhibitors: Synthesis, biological and in silico studies Bioorganic Chemistry. 2023. V.138. 106621 . DOI: 10.1016/j.bioorg.2023.106621 WOS Scopus OpenAlex
33	Karibov T.T. , Lichitsky B.V. , Komogortsev A.N. , Melekhina V.G. Amide moiety as analogue of double bond in aza-1,3,5-hexatriene system: Photochemical synthesis of benzofuro[3,2-c]isoquinolines Tetrahedron. 2023. V.141. 133497 . DOI: 10.1016/j.tet.2023.133497 WOS Scopus OpenAlex
34	Lichitsky B.V. , Komogortsev A.N. , Melekhina V.G. (2R,6′R,E)-3′-(1-Aminoethylidene)-7-chloro-4,6-dimethoxy-6′-methyl-3H-spiro[benzofuran-2,1′-cyclohexane]-2′,3,4′-trione Molbank. 2023. V.2023. N1. M1590 . DOI: 10.3390/m1590 WOS Scopus OpenAlex
35	Milyutin C.V. , Komogortsev A.N. , Melekhina V.G. , Lichitsky B.V. Synthesis of the substituted 7 H -pyrano[2,3- d ]isoxazol-7-ones from allomaltol-containing oximes Synthetic Communications. 2023. V.53. N24. P.2108-2116. DOI: 10.1080/00397911.2023.2272208 WOS Scopus OpenAlex
36	Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V. , Melekhina V.G. Acid‐catalyzed recyclization of spiroindolinepyrano[3,2‐b]pyrans to 3,4‐dihydroquinolinone derivatives containing allomaltol fragment Journal of Heterocyclic Chemistry. 2023. V.60. N8. P.1427-1436. DOI: 10.1002/jhet.4690 WOS Scopus OpenAlex
37	Komogortsev A.N. , Lichitsky B.V. , Melekhina V.G. Synthesis of substituted 2-arylfuro[3,2-b]pyrans via acid-catalyzed recyclization of 2-aminofurans containing allomaltol fragment Synthetic Communications. 2023. V.53. N10. P.720-730. DOI: 10.1080/00397911.2023.2191856 WOS Scopus OpenAlex
38	Karibov T.T. , Lichitsky B.V. , Melekhina V.G. , Komogortsev A.N. The First Example of Photogeneration of a Pyrrole Molecule on the Basis of 6π-Electrocyclization of 2-Arylbenzofurans Containing a Pyrazole Fragment Polycyclic Aromatic Compounds. 2023. V.43. N7. P.6160-6180. DOI: 10.1080/10406638.2022.2112706 WOS Scopus OpenAlex
39	Lichitsky B.V. , Karibov T.T. , Komogortsev A.N. , Melekhina V.G. N,N'-(2-aryl-2-oxoethane-1,1-diyl)diamides as convenient synthons for the preparation of 3-amido-2-arylbenzofurans Tetrahedron. 2023. V.132. 133244 . DOI: 10.1016/j.tet.2022.133244 WOS Scopus OpenAlex
40	Komogortsev A.N. , Lichitskii B. , Milyutin C.V. , Melekhina V. Photochemical synthesis and ring–chain–ring tautomerism of benzo[4,5]imidazo[1,2-a]cyclopenta[e]pyridines Organic & Biomolecular Chemistry. 2023. V.21. N13. P.2720-2728. DOI: 10.1039/d3ob00273j WOS Scopus OpenAlex
41	Komogortsev A.N. , Lichitsky B.V. , Melekhina V.G. Novel approach for the synthesis of 2-arylfuro[3,2-b]pyran-3-carbaldehydes based on acid-catalyzed cyclization of allomaltol containing enaminones Synthetic Communications. 2023. V.53. N1. P.58-67. DOI: 10.1080/00397911.2022.2150975 WOS Scopus OpenAlex
42	Karibov T.T. , Lichitsky B.V. , Komogortsev A.N. , Melekhina V.G. Photoinduced 6π‐electrocyclization of 2,5‐dichlorothiophene containing benzofuranylacrylonitriles as efficient method for the generation of hydrogen chloride Journal of Heterocyclic Chemistry. 2023. V.60. N2. P.264-276. DOI: 10.1002/jhet.4578 WOS Scopus OpenAlex
43	Komogortsev A.N. , Lichitskii B. , Melekhina V. 1,1′-Carbonyldiimidazole-mediated transformation of allomaltol containing hydrazides into substituted 3-acetyltetronic acids Organic & Biomolecular Chemistry. 2023. V.21. N35. P.7224-7230. DOI: 10.1039/d3ob01136d WOS Scopus OpenAlex
44	Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V. , Minyaev M.E. , Melekhina V.G. Synthesis of substituted 8H-benzo[h]pyrano[2,3-f]quinazolin-8-ones via photochemical 6π-electrocyclization of pyrimidines containing an allomaltol fragment Beilstein Journal of Organic Chemistry. 2023. V.19. P.778–788. DOI: 10.3762/bjoc.19.58 WOS Scopus OpenAlex
45	Komogortsev A.N. , Melekhina V.G. , Lichitsky B.V. , Migulin V.A. , Karibov T.T. , Minyaev M.E. The multicomponent synthesis of urea substituted 2-arylfurans Tetrahedron. 2022. V.111. 132716 . DOI: 10.1016/j.tet.2022.132716 WOS Scopus OpenAlex
46	Lichitsky B.V. , Komogortsev A.N. , Melekhina V.G. 2-(5-Acetyl-7-methoxy-2-(4-methoxyphenyl)benzofuran-3-yl)acetic Acid Molbank. 2022. V.2022. N2. M1357 . DOI: 10.3390/m1357 WOS Scopus OpenAlex
47	Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V. , Melekhina V.G. Investigation of photochemical behavior of furan derivatives containing an allomaltol fragment Tetrahedron. 2022. V.124. 133012 . DOI: 10.1016/j.tet.2022.133012 WOS Scopus OpenAlex
48	Milyutin C.V. , Galimova R.G. , Komogortsev A.N. , Lichitsky B.V. , Migulin V.A. , Melekhina V.G. Photochemical Synthesis of Tetrahydro‐6H‐cyclopenta[b]furan‐6‐ones from Substituted Allomaltols ChemistrySelect. 2022. V.7. N46. e202204000 . DOI: 10.1002/slct.202204000 WOS Scopus OpenAlex
49	Lichitsky B.V. , Komogortsev A.N. , Melekhina V.G. 3-Phenyl-10-(2,3,4-trimethoxyphenyl)-9,10-dihydro-4H,8H-pyrano [2,3-f]chromene-4,8-dione Molbank. 2022. V.2022. N4. M1516 . DOI: 10.3390/m1516 WOS Scopus OpenAlex
50	Kartsev V. , Geronikaki A. , Lichitsky B. , Komogortsev A. , Petrou A. , Ivanov M. , Glamočlija J. , Soković M. Synthesis, biological evaluation, and molecular docking studies of thiazolo[4,5‐b]pyridin‐5‐ones as antimicrobial agents Journal of Heterocyclic Chemistry. 2022. V.59. N9. P.1573-1590. DOI: 10.1002/jhet.4491 WOS Scopus OpenAlex

Conference attendances (3) More info

1	Angeli A. , Kartsev V. , Petrou A. , Lichitsky B. , Geronikaki A. , Supuran C.T. Pyrazolo[4,3-с]pyridine sulfonamides as carbonic anhydrase inhibitors: synthesis, biological and in silico studies The Seventh International Scientific Conference "Advances in Synthesis and Complexing" 29 Sep - 3 Oct 2025
2	Migulin A.V. , Komogortsev A.N. , Lichitsky B.V. , Milyutin K.V. Investigation of the photochemical behavior of allomaltol-containing 2-aminothiazole derivatives The Seventh International Scientific Conference "Advances in Synthesis and Complexing" 29 Sep - 3 Oct 2025
3	Geronikaki A. , Angeli A. , Kartsev V. , Petrou A. , Lichitsky B. , Supuran C.T. Pyrazolo[4,3-c]pyridine sulfonamides as carbonic anhydrase inhibitors: synthesis, biological and in silico studies New Emerging Trends in Chemistry 21-25 Sep 2025