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81
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Novikov R.A.
, Levina A.A.
, Borisov D.D.
, Volodin A.D.
, Korlyukov A.A.
, Tkachev Y.V.
, Platonova Y.B.
, Tomilova L.G.
, Tomilov Y.V.
Synthesis of the Cationic Gallium Phthalocyanines and Their Catalytic Application in Gallium(III)-Activated Processes for Donor–Acceptor Substrates
Organometallics. 2020.
V.39. N14. P.2580-2593. DOI: 10.1021/acs.organomet.0c00113
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82
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Novikov M.A.
, Bobrova A.Y.
, Mezentsev I.A.
, Medvedev M.G.
, Tomilov Y.V.
(2-Fluoroallyl)boration of Ketones with (2-Fluoroallyl)boronates
Journal of Organic Chemistry. 2020.
V.85. N10. P.6295-6308. DOI: 10.1021/acs.joc.9b03445
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83
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Shulishov E.V.
, Pantyukh O.A.
, Menchikov L.G.
, Tomilov Y.V.
Catalytic cyclopropanation of spiro[2.4]hepta-4,6-diene with diazomethane
Tetrahedron Letters. 2019.
V.60. N31. P.2043-2045. DOI: 10.1016/j.tetlet.2019.06.044
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84
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Borisov D.D.
, Chermashentsev G.R.
, Novikov R.A.
, Tomilov Y.V.
“Four-component” assembly of polyaromatic 4H-cyclopenta[b]thiophene structures based on GaCl3-promoted reaction of styrylmalonates with 5-phenylthiophene-2-carbaldehyde
Tetrahedron Letters. 2019.
V.60. N10. P.746-750. DOI: 10.1016/j.tetlet.2019.02.007
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85
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Borisova I.A.
, Tarasova A.V.
, Potapov K.V.
, Novikov R.A.
, Tomilov Y.V.
Reactions of donor-acceptor cyclopropanes or benzylidenemalonate with benzyl azide by generating gallium trichloride 1,2-zwitterionic complexes
Russian Chemical Bulletin. 2019.
V.68. N8. P.1504-1509. DOI: 10.1007/s11172-019-2584-2
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86
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Belyy A.Y.
, Levina A.A.
, Platonov D.N.
, Salikov R.F.
, Medvedev M.G.
, Tomilov Y.V.
Synthesis of Diazanorcaradienes and 1,2‐Diazepines via the Tandem [4+2]‐Cycloaddition/Retro‐[4+2]‐Cycloaddition Reaction between Methoxycarbonylcyclopropenes and Dimethoxycarbonyltetrazine
European Journal of Organic Chemistry. 2019.
V.2019. N26. P.4133-4138. DOI: 10.1002/ejoc.201801861
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87
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Trainov K.P.
, Litvinenko V.V.
, Salikov R.F.
, Platonov D.N.
, Tomilov Y.V.
Synthesis of chromophores based on the hydrazinylidene cyclic acceptor moieties via the reaction of organolithium reagents with diazo compounds
Dyes and Pigments. 2019.
V.170. 107589
. DOI: 10.1016/j.dyepig.2019.107589
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88
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Denisov D.A.
, Borisov D.D.
, Korolev V.A.
, Novikov R.A.
, Tomilov Y.V.
Three-Component GaHal3-Promoted Reactions of Substituted Methylidenemalonates and Donor–Acceptor Cyclopropanes with Propargyl Halides: Cascade Diastereoselective Construction of Five-Membered Lactones
Journal of Organic Chemistry. 2019.
V.84. N10. P.6174-6182. DOI: 10.1021/acs.joc.9b00354
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89
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Zotova M.A.
, Novikov R.A.
, Volodin A.D.
, Korlyukov A.A.
, Tkachev Y.V.
, Korolev V.A.
, Tomilov Y.V.
Four-Membered Cycle Formation Challenge: GaCl3 -Promoted Formal [2+2]-Cycloaddition of Donor-Acceptor Cyclopropanes to Bicyclobutylidene
European Journal of Organic Chemistry. 2019.
V.2019. N26. P.4207-4214. DOI: 10.1002/ejoc.201900329
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90
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Salikov R.F.
, Trainov K.P.
, Platonov D.N.
, Davydov D.A.
, Lee S.
, Gerasimov I.S.
, Medvedev M.G.
, Levina A.A.
, Belyy A.Y.
, Tomilov Y.V.
Synthesis and TD-DFT investigation of arylhydrazonocyclopentadiene dyes
Dyes and Pigments. 2019.
V.161. P.500-509. DOI: 10.1016/j.dyepig.2018.09.040
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91
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Trainov K.P.
, Salikov R.F.
, Luponosov Y.N.
, Savchenko P.S.
, Mannanov A.L.
, Ponomarenko S.A.
, Platonov D.N.
, Tomilov Y.V.
Push-pull molecules bearing a hydrazonocyclopentadiene acceptor moiety: from the synthesis to organic photovoltaic applications
Mendeleev Communications. 2019.
V.29. N3. P.304-306. DOI: 10.1016/j.mencom.2019.05.021
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92
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Denisov D.A.
, Borisov D.D.
, Potapov K.V.
, Novikov R.A.
, Tomilov Y.V.
4-Phenylspiro[2.2]pentane-1,1-dicarboxylate: synthesis and reactions with EtAlCl2 and 4,5-diazaspiro[2.4]hept-4-ene derivative
Mendeleev Communications. 2019.
V.29. N4. P.417-418. DOI: 10.1016/j.mencom.2019.07.020
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93
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Novikov R.A.
, Borisov D.D.
, Zotova M.A.
, Denisov D.A.
, Tkachev Y.V.
, Korolev V.A.
, Shulishov E.V.
, Tomilov Y.V.
Cascade Cleavage of Three-Membered Rings in the Reaction of D–A Cyclopropanes with 4,5-Diazaspiro[2.4]hept-4-enes: A Route to Highly Functionalized Pyrazolines
Journal of Organic Chemistry. 2018.
V.83. N15. P.7836-7851. DOI: 10.1021/acs.joc.8b00725
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94
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Gibadullina N.N.
, Latypova D.R.
, Vakhitov V.A.
, Khasanova D.V.
, Zainullina L.F.
, Vakhitova Y.V.
, Lobov A.N.
, Ugrak B.I.
, Tomilov Y.V.
, Dokichev V.A.
Synthesis and cytotoxic activities of difluoroacetyl-substituted hexahydropyrimidine derivatives
Journal of Fluorine Chemistry. 2018.
V.211. P.94-99. DOI: 10.1016/j.jfluchem.2018.04.011
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95
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Belyy A.Y.
, Platonov D.N.
, Salikov R.F.
, Levina A.A.
, Tomilov Y.V.
A New Simple Procedure for the Synthesis of Heptamethyl Cyclohepta-1,3,5-triene-1,2,3,4,5,6,7-heptacarboxylate
Synlett. 2018.
V.29. N09. P.1157-1160. DOI: 10.1055/s-0036-1591962
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96
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Salikov R.F.
, Trainov K.P.
, Belousova I.K.
, Belyy A.Y.
, Fatkullina U.S.
, Mulyukova R.V.
, Zainullina L.F.
, Vakhitova Y.V.
, Tomilov Y.V.
Branching tryptamines as a tool to tune their antiproliferative activity
European Journal of Medicinal Chemistry. 2018.
V.144. P.211-217. DOI: 10.1016/j.ejmech.2017.12.028
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97
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Salikov R.F.
, Trainov K.P.
, Platonov D.N.
, Belyy A.Y.
, Tomilov Y.V.
Synthesis of 1,2,3,4,5‐Penta(methoxycarbonyl)cyclopentadienides through Electrocyclic Ring Closure and Ring Contraction Reactions
European Journal of Organic Chemistry. 2018.
V.2018. N36. P.5065-5068. DOI: 10.1002/ejoc.201800732
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98
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Novikov R.A.
, Borisov D.D.
, Tarasova A.V.
, Tkachev Y.V.
, Tomilov Y.V.
Three‐Component Gallium(III)‐Promoted Addition of Halide Anions and Acetylenes to Donor–Acceptor Cyclopropanes
Angewandte Chemie International Edition. 2018.
V.57. N32. P.10293-10298. DOI: 10.1002/anie.201803541
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99
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Novikov R.A.
, Borisov D.D.
, Tomilov Y.V.
Lewis acid-mediated reactions of donor-acceptor cyclopropanes with diazo esters
Russian Chemical Bulletin. 2018.
V.67. N2. P.265-273. DOI: 10.1007/s11172-018-2069-8
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100
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Novikov R.A.
, Denisov D.A.
, Potapov K.V.
, Tkachev Y.V.
, Shulishov E.V.
, Tomilov Y.V.
Ionic Ga-Complexes of Alkylidene- and Arylmethylidenemalonates and Their Reactions with Acetylenes: An In-Depth Look into the Mechanism of the Occurring Gallium Chemistry
Journal of the American Chemical Society. 2018.
V.140. N43. P.14381-14390. DOI: 10.1021/jacs.8b08913
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