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61
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Milyutin C.V.
, Komogortsev A.N.
, Lichitsky B.V.
, Melekhina V.G.
, Minyaev M.E.
Construction of Spiro-γ-butyrolactone Core via Cascade Photochemical Reaction of 3-Hydroxypyran-4-one Derivatives
Organic Letters. 2021.
V.23. N13. P.5266-5270. DOI: 10.1021/acs.orglett.1c01814
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62
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Komogortsev A.N.
, Lichitsky B.V.
, Melekhina V.G.
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Photoinduced 6π-Electrocyclization of a 1,3,5-Hexatriene System Containing an Allomaltol Fragment
Journal of Organic Chemistry. 2021.
V.86. N21. P.15345-15356. DOI: 10.1021/acs.joc.1c01902
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63
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Kostenko A.A.
, Bykova K.A.
, Kucherenko A.S.
, Komogortsev A.N.
, Lichitsky B.V.
, Zlotin S.G.
2-Nitroallyl carbonate-based green bifunctional reagents for catalytic asymmetric annulation reactions
Organic & Biomolecular Chemistry. 2021.
V.19. N8. P.1780-1786. DOI: 10.1039/d0ob02283g
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64
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Lichitsky B.V.
, Milyutin C.V.
, Melekhina V.G.
, Fakhrutdinov A.N.
, Komogortsev A.N.
, Krayushkin M.M.
Photochemical synthesis of novel naphtho[1,2-b]benzofuran derivatives from 2,3-disubstituted benzofurans
Chemistry of Heterocyclic Compounds. 2021.
V.57. N1. P.13-19. DOI: 10.1007/s10593-021-02861-2
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65
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Lichitskii B.V.
, Melekhina V.G.
, Komogortsev A.N.
, Milyutin C.V.
, Fakhrutdinov A.N.
, Gorbunov Y.O.
, Krayushkin M.M.
Synthesis of substituted naphtho[1,2-b]benzofuran-7(8H)-ones via photoinduced rearrangement of 4H-chromen-4-one derivatives
Organic & Biomolecular Chemistry. 2020.
V.18. N13. P.2501-2509. DOI: 10.1039/d0ob00149j
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66
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Komogortsev A.N.
, Melekhina V.G.
, Lichitsky B.V.
, Minyaev M.E.
Novel one-pot approach to 2-aminofuran derivatives via multicomponent reaction of 3-hydroxy-4H-pyran-4-ones, α-ketoaldehydes and methylene active nitriles
Tetrahedron Letters. 2020.
V.61. N41. 152384
. DOI: 10.1016/j.tetlet.2020.152384
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67
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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
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68
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Komogortsev A.N.
, Melekhina V.G.
, Lichitsky B.V.
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Synthesis of hydroxy-containing terarylenes with pyrazole and allomaltol fragments
Russian Chemical Bulletin. 2020.
V.69. N4. P.758-762. DOI: 10.1007/s11172-020-2829-0
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69
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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
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70
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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
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71
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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
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72
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Lichitsky B.V.
, Tretyakov А.D.
, Komogortsev A.N.
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, 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
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73
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Kutasevich A.V.
, Perevalov V.P.
, Mityanov V.S.
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, 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
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74
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Kucherenko A.S.
, Kostenko A.A.
, Komogortsev A.N.
, Lichitsky B.V.
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, 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
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75
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Melekhina V.G.
, Mityanov V.S.
, Lichitsky B.V.
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, 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
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76
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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
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77
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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
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78
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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
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79
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Komogortsev A.N.
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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
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80
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Komogortsev A.N.
, Lichitsky B.V.
, Tretyakov A.D.
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, 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
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