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21
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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
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22
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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
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23
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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
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24
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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
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25
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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
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26
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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
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27
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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
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28
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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
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29
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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
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30
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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
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31
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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
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32
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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
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33
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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
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34
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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
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35
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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
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36
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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
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37
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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
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38
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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
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39
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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
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40
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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
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