Articles - Sciact

Articles (108)

#	Публикация
21	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
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	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	Komogortsev A.N. , Milyutin C.V. , Lichitsky B.V. , Melekhina V.G. Photoinduced 6π-Electrocyclization of 1,3,5-hexatriene system containing allomaltol fragment: A convenient approach to polycondensed pyrrole derivatives Tetrahedron. 2022. V.114. 132780 . DOI: 10.1016/j.tet.2022.132780 WOS Scopus OpenAlex
40	Milyutin C.V. , Komogortsev A.N. , Lichitsky B.V. , Melekhina V.G. A study of the photochemical behavior of terarylenes containing allomaltol and pyrazole fragments Beilstein Journal of Organic Chemistry. 2022. V.18. P.588-596. DOI: 10.3762/bjoc.18.61 WOS Scopus OpenAlex

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