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81
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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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82
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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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83
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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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84
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Zotova M.A.
, Novikov R.A.
, Shulishov E.V.
, Tomilov Y.V.
GaCl3-Mediated “Inverted” Formal [3 + 2]-Cycloaddition of Donor–Acceptor Cyclopropanes to Allylic Systems
Journal of Organic Chemistry. 2018.
V.83. N15. P.8193-8207. DOI: 10.1021/acs.joc.8b00959
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85
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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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86
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Salikov R.F.
, Trainov K.P.
, Levina A.A.
, Belousova I.K.
, Medvedev M.G.
, Tomilov Y.V.
Synthesis of Branched Tryptamines via the Domino Cloke–Stevens/Grandberg Rearrangement
Journal of Organic Chemistry. 2017.
V.82. N1. P.790-795. DOI: 10.1021/acs.joc.6b02578
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87
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Borisov D.D.
, Novikov R.A.
, Eltysheva A.S.
, Tkachev Y.V.
, Tomilov Y.V.
Styrylmalonates as an Alternative to Donor–Acceptor Cyclopropanes in the Reactions with Aldehydes: A Route to 5,6-Dihydropyran-2-ones
Organic Letters. 2017.
V.19. N14. P.3731-3734. DOI: 10.1021/acs.orglett.7b01556
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88
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Borisov D.D.
, Novikov R.A.
, Tomilov Y.V.
Highly diastereoselective formation of 3,7-dioxabicyclo[3.3.0]octan-2-ones in reaction of 2-arylcyclopropanedicarboxylates with aromatic aldehydes using 1,2-zwitterionic reactivity type
Tetrahedron Letters. 2017.
V.58. N38. P.3712-3716. DOI: 10.1016/j.tetlet.2017.08.025
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89
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Gibadullina N.N.
, Latypova D.R.
, Novikov R.A.
, Tomilov Y.V.
, Dokichev V.A.
Reaction of trifluoromethyl 1,3-dicarbonyl compounds with formaldehyde and esters of natural α-aminoacids
Arkivoc. 2017.
N4. P.222-235. DOI: 10.24820/ark.5550190.p010.003
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90
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Ananikov V.P.
, Eremin D.B.
, Yakukhnov S.A.
, Dilman A.D.
, Levin V.V.
, Egorov M.P.
, Karlov S.S.
, Kustov L.M.
, Tarasov A.L.
, Greish A.A.
, Shesterkina A.A.
, Sakharov A.M.
, Nysenko Z.N.
, Sheremetev A.B.
, Stakheev A.Y.
, Mashkovsky I.S.
, Sukhorukov A.Y.
, Ioffe S.L.
, Terent’ev A.O.
, Vil V.A.
, Tomilov Y.V.
, Novikov R.A.
, Zlotin S.G.
, Kucherenko A.S.
, Ustyuzhanina N.E.
, Krylov V.B.
, Tsvetkov Y.E.
, Gening M.L.
, Nifantiev N.E.
Organic and hybrid systems: from science to practice
Mendeleev Communications. 2017.
V.27. N5. P.425-438. DOI: 10.1016/j.mencom.2017.09.001
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91
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Novikov R.A.
, Tarasova A.V.
, Denisov D.A.
, Borisov D.D.
, Korolev V.A.
, Timofeev V.P.
, Tomilov Y.V.
[4 + 2] Annulation of Donor–Acceptor Cyclopropanes with Acetylenes Using 1,2-Zwitterionic Reactivity
Journal of Organic Chemistry. 2017.
V.82. N5. P.2724-2738. DOI: 10.1021/acs.joc.7b00209
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92
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Borisov D.D.
, Novikov R.A.
, Tomilov Y.V.
GaCl3‐Mediated Reactions of Donor–Acceptor Cyclopropanes with Aromatic Aldehydes
Angewandte Chemie International Edition. 2016.
V.55. N40. P.12233-12237. DOI: 10.1002/anie.201603927
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93
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Novikov R.A.
, Tarasova A.V.
, Denisov D.A.
, Korolev V.A.
, Tomilov Y.V.
Cascade dimerization of 2-styryl-1,1-cyclopropanedicarboxylate upon treatment with gallium trichloride
Russian Chemical Bulletin. 2016.
V.65. N11. P.2628-2638. DOI: 10.1007/s11172-016-1628-0
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94
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Platonov D.N.
, Okonnishnikova G.P.
, Salikov R.F.
, Tomilov Y.V.
Synthesis and UV–vis spectra of a new type of dye via a decarboxylative azo coupling reaction
Tetrahedron Letters. 2016.
V.57. N38. P.4311-4313. DOI: 10.1016/j.tetlet.2016.08.043
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95
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Denisov D.A.
, Novikov R.A.
, Potapov K.V.
, Korolev V.A.
, Shulishov E.V.
, Tomilov Y.V.
1,1 ’-Bicyclopropyl-2,2-dicarboxylate and Cyclopropylmethylidenemalonate as Homovinylogs and Vinylogs of Donor-Acceptor Cyclopropanes
ChemistrySelect. 2016.
V.1. N20. P.6374-6381. DOI: 10.1002/slct.201601506
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96
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Platonov D.N.
, Belyy A.Y.
, Ananyev I.V.
, Tomilov Y.V.
Synthesis of 1,2,3,4,5,6,7-Heptasubstituted Cycloheptatrienes through Cycloaddition Reactions of Substituted Cyclopentadienones
European Journal of Organic Chemistry. 2016.
V.2016. N23. P.4105-4110. DOI: 10.1002/ejoc.201600516
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97
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Fakhreeva A.V.
, Gusakov V.N.
, Voloshin A.I.
, Tomilov Y.V.
, Nifant’ev N.E.
, Dokichev V.A.
Effect of sodium-carboxymethylcellulose on inhibition of scaling by calcium carbonate and sulfate
Russian Journal of Applied Chemistry. 2016.
V.89. N12. P.1955-1959. DOI: 10.1134/s1070427216120053
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98
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Novikov R.A.
, Borisov D.D.
, Tomilov Y.V.
The effect of ligands on the change of diastereoselectivity dimerization of 2-(naphthyl-1)cyclopropanedicarboxylate in the presence of GaCl3
Arkivoc. 2016.
N5. P.362-375. DOI: 10.24820/ark.5550190.p009.860
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99
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Novikov R.A.
, Tarasova A.V.
, Tomilov Y.V.
GaCl3-Mediated Isomerization of Donor–Acceptor Cyclopropanes into (2-Arylalkylidene)malonates
Synlett. 2016.
V.27. N09. P.1367-1370. DOI: 10.1055/s-0035-1561389
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100
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Novikov R.A.
, Tomilov Y.V.
Dimerization of donor–acceptor cyclopropanes
Mendeleev Communications. 2015.
V.25. N1. P.1-10. DOI: 10.1016/j.mencom.2015.01.001
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