Статьи - Sciact

Статьи (153)

#	Публикация
81	Lichitsky B.V. , Melekhina V.G. , Komogortsev A.N. , Minyaev M.E. A new multicomponent approach to the synthesis of substituted furan-2(5H)-ones containing 4H-chromen-4-one fragment Tetrahedron Letters. 2020. V.61. N49. 152602 . DOI: 10.1016/j.tetlet.2020.152602 WOS Scopus OpenAlex
82	Milyutin C.V. , Lichitsky B.V. , Melekhina V.G. , Komogortsev A.N. , Fakhrutdinov A.N. , Minyaev M.E. , Krayushkin M.M. Synthesis of 1H-pyrano[4,3-b]benzofuran-1-one derivatives via photochemical cyclization of substituted 4H-furo[3,2-c]pyran-4-ones Tetrahedron Letters. 2020. V.61. N44. 152469 . DOI: 10.1016/j.tetlet.2020.152469 WOS Scopus OpenAlex
83	Geronikaki A. , Kartsev V. , Petrou A. , Akrivou M.G. , Vizirianakis I.S. , Chatzopoulou F.M. , Lichitsky B. , Sirakanyan S. , Kostic M. , Smiljkovic M. , Soković M. , Druzhilovskiy D. , Poroikov V. Antibacterial activity of griseofulvin analogues as an example of drug repurposing International Journal of Antimicrobial Agents. 2020. V.55. N3. 105884 . DOI: 10.1016/j.ijantimicag.2020.105884 WOS Scopus OpenAlex
84	Perevalov V.P. , Mityanov V.S. , Lichitsky B.V. , Komogortsev A.N. , Kuz’mina L.G. , Koldaeva T.Y. , Miroshnikov V.S. , Kutasevich A.V. Synthesis of highly functional imidazole derivatives via assembly of 2-unsubstituted imidazole N-oxides with CH-acids and arylglyoxals Tetrahedron. 2020. V.76. N8. 130947 . DOI: 10.1016/j.tet.2020.130947 WOS Scopus OpenAlex
85	Lichitsky B.V. , Tretyakov A.D. , Komogortsev A.N. , Mityanov V.S. , Dudinov A.A. , Gorbunov Y.O. , Daeva E.D. , Krayushkin M.M. Synthesis of substituted benzofuran-3-ylacetic acids based on three-component condensation of polyalkoxyphenols, arylglyoxals and Meldrum's acid Mendeleev Communications. 2019. V.29. N5. P.587-588. DOI: 10.1016/j.mencom.2019.09.037 WOS Scopus OpenAlex
86	Kartsev V. , Geronikaki A. , Bua S. , Nocentini A. , Petrou A. , Lichitsky B. , Frasinyuk M. , Leitans J. , Kazaks A. , Tars K. , Supuran C.T. Extending the Inhibition Profiles of Coumarin-Based Compounds Against Human Carbonic Anhydrases: Synthesis, Biological, and In Silico Evaluation Molecules. 2019. V.24. N19. 3580 . DOI: 10.3390/molecules24193580 WOS Scopus OpenAlex
87	Melekhina V.G. , Komogortsev A.N. , Lichitsky B.V. , Mityanov V.S. , Fakhrutdinov A.N. , Dudinov A.A. , Migulin V.A. , Nelyubina Y.V. , Melnikova E.K. , Krayushkin M.M. One-pot synthesis of substituted pyrrolo[3,4-b]pyridine-4,5-diones based on the reaction of N-(1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-2-oxo-2-arylethyl)acetamide with amines Beilstein Journal of Organic Chemistry. 2019. V.15. P.2840-2846. DOI: 10.3762/bjoc.15.277 WOS Scopus OpenAlex
88	Lichitsky B.V. , Tretyakov А.D. , Komogortsev A.N. , Mityanov V.S. , Dudinov A.А. , Krayushkin M.M. Synthesis of Substituted Imidazo[1,2-a]Pyridin-3-yl-Acetic Acids by Multicomponent Condensation of 2-Aminopyridines with Arylglyoxals and Meldrum’s Acid Chemistry of Heterocyclic Compounds. 2019. V.55. N2. P.156-159. DOI: 10.1007/s10593-019-02432-6 WOS Scopus OpenAlex
89	Kutasevich A.V. , Perevalov V.P. , Mityanov V.S. , Lichitsky B.V. , Komogortsev A.N. , Krayushkin M.M. , Koldaeva T.Y. , Miroshnikov V.S. A new facile method for the synthesis of 3-imidazolylpropionic acid N-oxides Chemistry of Heterocyclic Compounds. 2019. V.55. N2. P.147-155. DOI: 10.1007/s10593-019-02431-7 WOS Scopus OpenAlex
90	Kucherenko A.S. , Kostenko A.A. , Komogortsev A.N. , Lichitsky B.V. , Fedotov M.Y. , Zlotin S.G. C2-Symmetric Chiral Squaramide, Recyclable Organocatalyst for Asymmetric Michael Reactions Journal of Organic Chemistry. 2019. V.84. N7. P.4304-4311. DOI: 10.1021/acs.joc.9b00252 WOS Scopus OpenAlex
91	Melekhina V.G. , Mityanov V.S. , Lichitsky B.V. , Komogortsev A.N. , Lyssenko K.A. , Krayushkin M.M. Synthesis of Benzocarbazole Derivatives by Photocyclization European Journal of Organic Chemistry. 2019. V.2019. N6. P.1335-1340. DOI: 10.1002/ejoc.201801664 WOS Scopus OpenAlex
92	Melekhina V.G. , Mityanov V.S. , Lichitsky B.V. , Komogortsev A.N. , Fakhrutdinov A.N. , Daeva E.D. , Krayushkin M.M. Ultraviolet irradiation of terarylenes: A facile, efficient, and environmentally friendly method for the synthesis of fused polycyclic products Tetrahedron Letters. 2019. V.60. N26. P.1745-1747. DOI: 10.1016/j.tetlet.2019.05.063 WOS Scopus OpenAlex
93	Kartsev V. , Geronikaki A. , Petrou A. , Lichitsky B. , Kostic M. , Smiljkovic M. , Soković M. , Sirakanyan S. Griseofulvin Derivatives: Synthesis, Molecular Docking and Biological Evaluation Current Topics in Medicinal Chemistry. 2019. V.19. N13. P.1145-1161. DOI: 10.2174/1568026619666190523080136 WOS Scopus OpenAlex
94	Melekhina V.G. , Komogortsev A.N. , Lichitsky B.V. , Mityanov V.S. , Fakhrutdinov A.N. , Dudinov A.A. , Migulin V.A. , Nelyubina Y.V. , Melnikova E.K. , Krayushkin M.M. Unexpected photochemical transformation of imidazole derivatives containing the 5-hydroxy-2-methyl-4H-pyran-4-one moiety. Environmentally friendly method for the synthesis of substituted imidazo[1,5-a]pyridine-5,8-diones Tetrahedron Letters. 2019. V.60. N39. 151080 . DOI: 10.1016/j.tetlet.2019.151080 WOS Scopus OpenAlex
95	Lichitsky B.V. , Komogortsev A.N. , Dudinov A.A. , Krayushkin M.M. , Khodot E.N. , Samet A.V. , Silyanova E.A. , Konyushkin L.D. , Karpov A.S. , Gorses D. , Radimerski T. , Semenova M.N. , Kiselyov A.S. , Semenov V.V. Benzimidazolyl-pyrazolo[3,4-b]pyridinones, Selective Inhibitors of MOLT-4 Leukemia Cell Growth and Sea Urchin Embryo Spiculogenesis: Target Quest ACS Combinatorial Science. 2019. V.21. N12. P.805-816. DOI: 10.1021/acscombsci.9b00135 WOS Scopus OpenAlex
96	Krylov C.S. , Komogortsev A.N. , Lichitsky B.V. , Fakhrutdinov A.N. , Dudinov A.А. , Krayushkin M.M. Three-Component Condensation of 4-Imino-1-Phenylimidazolidin-2-One with Aldehydes and Meldrum's Acid: Synthesis of Imidazo[4,5-b]Pyridine-2,5(4H,6H)-Diones and 5-Substituted 1-Phenylhydantoins Chemistry of Heterocyclic Compounds. 2019. V.55. N9. P.851-855. DOI: 10.1007/s10593-019-02548-9 WOS Scopus OpenAlex
97	Komogortsev A.N. , Lichitsky B.V. , Tretyakov A.D. , Dudinov A.A. , Krayushkin M.M. Investigation of the multicomponent reaction of 5-hydroxy-2-methyl-4H-pyran-4-one with carbonyl compounds and Meldrum's acid Chemistry of Heterocyclic Compounds. 2019. V.55. N9. P.818-822. DOI: 10.1007/s10593-019-02542-1 WOS Scopus OpenAlex
98	Komogortsev A.N. , Lichitsky B.V. , Tretyakov A.D. , Fakhrutdinov A.N. , Dudinov A.A. , Krayushkin M.M. New approach to the synthesis of substituted 7H‐furo[3,2‐b]pyran‐7‐ones based on 5‐hydroxy‐2‐methyl‐4H‐pyran‐4‐one derivatives Journal of Heterocyclic Chemistry. 2019. V.56. N11. P.3081-3087. DOI: 10.1002/jhet.3706 WOS Scopus OpenAlex
99	Kostenko A.A. , Kucherenko A.S. , Komogortsev A.N. , Lichitsky B.V. , Zlotin S.G. Asymmetric Michael addition between kojic acid derivatives and unsaturated ketoesters promoted by C2-symmetric organocatalysts Organic & Biomolecular Chemistry. 2018. V.16. N48. P.9314-9318. DOI: 10.1039/c8ob02523a WOS Scopus OpenAlex
100	Victor K. , Boris L. , Athina G. , Anthi P. , Marija S. , Marina K. , Oliver R. , Marina S. Design, synthesis and antimicrobial activity of usnic acid derivatives MedChemComm. 2018. V.9. N5. P.870-882. DOI: 10.1039/c8md00076j OpenAlex

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