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Articles (266)

# Публикация
61 Trainov K.P. , Chechekina O.G. , Salikov R.F. , Platonov D.N. , Tomilov Y.V.
Electron deficient cyclopentadienolate in the synthesis of chromophores with mono- and poly-cyclic hydrazonocyclopentadiene acceptor moieties
Dyes and Pigments. 2021. V.187. 109132 . DOI: 10.1016/j.dyepig.2020.109132 WOS Scopus OpenAlex
62 Denisov D.A. , Novikov R.A. , Tomilov Y.V.
Lewis acid mediated Michael addition of non-aromatic multiple C C bonds to α,β-unsaturated dicarbonyl compounds
Tetrahedron Letters. 2021. V.80. 153272 . DOI: 10.1016/j.tetlet.2021.153272 WOS Scopus OpenAlex
63 Belaya M.A. , Denisov D.A. , Novikov R.A. , Tomilov Y.V.
Aluminum chloride-catalyzed Diels-Adler reaction involving arylmethylidenemalonates and conjugated dienes
Russian Chemical Bulletin. 2021. V.70. N8. P.1537-1542. DOI: 10.1007/s11172-021-3249-5 WOS Scopus OpenAlex
64 Platonov D.N. , Kholodkov D.N. , Goncharova I.K. , Belaya M.A. , Tkachev Y.V. , Dorovatovskii P.V. , Volodin A.D. , Korlyukov A.A. , Tomilov Y.V. , Arzumanyan A.V. , Novikov R.A.
Ionic Cyclopropenium-Derived Triplatinum Cluster Complex [(Ph3C3)2Pt3(MeCN)4]2+(BF4–)2: Synthesis, Structure, and Perspectives for Use as a Catalyst for Hydrosilylation Reactions
Organometallics. 2021. V.40. N23. P.3876-3885. DOI: 10.1021/acs.organomet.1c00291 WOS Scopus OpenAlex
65 Bobrova A.Y. , Novikov M.A. , Tomilov Y.V.
(2-Fluoroallyl)pyridinium tetrafluoroborates: novel fluorinated electrophiles for Pd-catalyzed allylic substitution
Organic & Biomolecular Chemistry. 2021. V.19. N21. P.4678-4684. DOI: 10.1039/d1ob00567g WOS Scopus OpenAlex
66 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 WOS Scopus OpenAlex
67 Potapov K.V. , Denisov D.A. , Glushkova V.V. , Novikov R.A. , Tomilov Y.V.
Donor–Acceptor Bicyclopropyls as 1,6-Zwitterionic Intermediates: Synthesis and Reactions with 4-Phenyl-1,2,4-triazoline-3,5-dione and Terminal Acetylenes
Journal of Organic Chemistry. 2020. V.85. N23. P.15562-15576. DOI: 10.1021/acs.joc.0c02293 WOS Scopus OpenAlex
68 Shulishov E.V. , Pantyukh O.A. , Menchikov L.G. , Tomilov Y.V.
Unusual Side Transformation of Spiro[2,4]hepta‐4,6‐dienes into Fulvene Derivatives During Pd‐Catalyzed Cyclopropanation with Diazomethane
ChemistrySelect. 2020. V.5. N13. P.4046-4049. DOI: 10.1002/slct.202000160 WOS Scopus OpenAlex
69 Trainov K.P. , Salikov R.F. , Platonov D.N. , Tomilov Y.V.
Indacenodithienothiophene based chromophore with cyclopentadienylidenehydrazine acceptor moieties
Mendeleev Communications. 2020. V.30. N5. P.647-649. DOI: 10.1016/j.mencom.2020.09.032 WOS Scopus OpenAlex
70 Bobrova A.Y. , Novikov M. , Mezentsev I.A. , Tomilov Y.V.
(2-Fluoroallyl)palladium Complexes as Intermediates in Pd-Catalyzed Tsuji-Trost 2-Fluoroallylations: Synthesis and Reactivity
Journal of Fluorine Chemistry. 2020. V.236. 109553 . DOI: 10.1016/j.jfluchem.2020.109553 WOS Scopus OpenAlex
71 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 WOS Scopus OpenAlex
72 Shulishov E.V. , Pantyukh O.A. , Menchikov L.G. , Tomilov Y.V.
Pathways of Pd-catalyzed cyclopropanation of tetrahydroindene with diazomethane
Mendeleev Communications. 2020. V.30. N5. P.612-614. DOI: 10.1016/j.mencom.2020.09.020 WOS Scopus OpenAlex
73 Belaya M.A. , Knyazev D.A. , Novikov R.A. , Tomilov Y.V.
“Diels-Alder reaction” in the ionic version: GaCl3-promoted formation of substituted cyclohexenes from donor–acceptor cyclopropanes and dienes
Tetrahedron Letters. 2020. V.61. N25. 151990 . DOI: 10.1016/j.tetlet.2020.151990 WOS Scopus OpenAlex
74 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 Scopus OpenAlex
75 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 WOS Scopus OpenAlex
76 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 WOS Scopus OpenAlex
77 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 WOS Scopus OpenAlex
78 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 WOS Scopus OpenAlex
79 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 WOS Scopus OpenAlex
80 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 WOS Scopus OpenAlex

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