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Articles (271)

# Публикация
81 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
82 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
83 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
84 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
85 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 WOS Scopus OpenAlex
86 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 WOS Scopus OpenAlex
87 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 WOS Scopus OpenAlex
88 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
89 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 WOS Scopus OpenAlex
90 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 WOS Scopus OpenAlex
91 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 WOS Scopus OpenAlex
92 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 WOS Scopus OpenAlex
93 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 WOS Scopus OpenAlex
94 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 WOS Scopus OpenAlex
95 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 WOS Scopus OpenAlex
96 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 WOS Scopus OpenAlex
97 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 WOS Scopus OpenAlex
98 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 WOS Scopus OpenAlex
99 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 WOS Scopus OpenAlex
100 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 WOS Scopus OpenAlex

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