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Articles (113)

# Публикация
1 Самигуллина А.И. , Иванова Н.М. , Милютин К.В. , Комогорцев А.Н.
Молекулярная и кристаллическая структура трёх кристаллосольватов производного азаспиро[4.5]дец-7-ен-2,9-диона
Журнал структурной химии. 2026. Т.67. №9. 171219 . DOI: 10.26902/jsc_id171219 OpenAlex
2 Samigullina A.I. , Ivanova N.M. , Milyutin K.V. , Komogortsev A.N.
Molecular and Crystal Structure of Three Crystal Solvates of an Azaspiro[4.5]dec-7-Ene-2,9-Dione Derivative
Journal of Structural Chemistry. 2026. V.67. N9. P.1944-1953. DOI: 10.1134/s0022476626090064 WOS Scopus OpenAlex
3 Migulin A.V. , Milyutin C.V. , Komogortsev A.N.
Novel Photoacid Generators Derived From Allomaltol Containing Terarylenes With 2‐Aminooxazole Fragment
Journal of Heterocyclic Chemistry. 2026. V.63. N4. P.579-589. DOI: 10.1002/jhet.70157 WOS Scopus OpenAlex
4 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
5 Migulin A.V. , Milyutin C.V. , Komogortsev A.N.
Synthesis of allomaltol containing pyridazines and their photochemical transformation into substituted benzo[ h ]pyrano[2,3- f ]cinnolin-8-ones
Organic & Biomolecular Chemistry. 2026. V.24. P.2971-2980. DOI: 10.1039/d6ob00173d WOS Scopus OpenAlex
6 Kudryavtseva T.A. , Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V.
Assembly of 3,5-Dihydroxy-4H-selenopyran-4-one Core via Recyclization of Allomaltol Derivatives under Action of Triselenium Dicyanide
Organometallics. 2026. V.45. N9. P.1063–1070. DOI: 10.1021/acs.organomet.6c00037 WOS Scopus OpenAlex
7 Garbuzova M.R. , Milyutin C.V. , Komogortsev A.N.
Two‐Step Ring‐Transformation Strategy Toward Allomaltol Containing Pyrazolo[1,5‐ a ][1,3,5]Triazine‐2,4‐Diones From Pyrano[2,3‐ f ]Pyrazolo[3,4‐ d ][1,3]Oxazepines via Urea Intermediates
Journal of Heterocyclic Chemistry. 2026. V.63. N8. P.1300-1312. DOI: 10.1002/jhet.70215 WOS Scopus OpenAlex
8 Komogortsev A.N. , Milyutin C.V. , Kuzmina A.G.
Base-controlled divergent oxidative dimerization of allomaltol-containing enolates: access to distinct diastereomers of 1,4-diketones
Organic & Biomolecular Chemistry. 2026. V.24. N36. P.7654–7663. DOI: 10.1039/d6ob00932h WOS Scopus OpenAlex
9 Migulin A.V. , Migulin V.A. , Milyutin C.V. , Komogortsev A.N.
Photochemical Approach to Fused Quinoxaline Derivatives From Allomaltol‐Containing Terarylenes With 2‐Aminooxazole Bridge Fragment via Trapping of Unstable Cyclopentene‐1,2‐Dione Intermediates
Journal of Heterocyclic Chemistry. 2026. V.63. N10. P.1601-1610. DOI: 10.1002/jhet.70232 WOS Scopus OpenAlex
10 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
11 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
12 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
13 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
14 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
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 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
17 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
18 Garbuzova M.R. , Milyutin C.V. , Komogortsev A.N.
Efficient method for the synthesis of novel pyrano[2,3- f ]pyrazolo[3,4- d ][1,3]oxazepines from allomaltol containing pyrazoles
Synthetic Communications. 2025. V.55. N22. P.1680-1691. DOI: 10.1080/00397911.2025.2589481 WOS Scopus OpenAlex
19 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
20 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

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