|
41
|
Boichenko M.A.
, Plodukhin A.Y.
, Shorokhov V.V.
, Lebedev D.S.
, Filippova A.V.
, Zhokhov S.S.
, Tarasenko E.A.
, Rybakov V.B.
, Trushkov I.V.
, Ivanova O.A.
Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines
Molecules. 2022.
V.27. N23. 8468
. DOI: 10.3390/molecules27238468
WOS
Scopus
OpenAlex
|
|
42
|
Shcherbakov R.O.
, Eshmemet’eva D.A.
, Merkushev A.A.
, Trushkov I.V.
, Uchuskin M.G.
Transformation of 3-(Furan-2-yl)-1,3-di(het)arylpropan-1-ones to Prop-2-en-1-ones via Oxidative Furan Dearomatization/2-Ene-1,4,7-triones Cyclization
Molecules. 2021.
V.26. N9. 2637
. DOI: 10.3390/molecules26092637
WOS
Scopus
OpenAlex
|
|
43
|
Chalikidi P.N.
, Magkoev T.T.
, Gutnov A.V.
, Demidov O.P.
, Uchuskin M.G.
, Trushkov I.V.
, Abaev V.T.
One-Step Synthesis of Triphenylphosphonium Salts from (Het)arylmethyl Alcohols
Journal of Organic Chemistry. 2021.
V.86. N14. P.9838-9846. DOI: 10.1021/acs.joc.1c00733
WOS
Scopus
OpenAlex
|
|
44
|
Boichenko M.А.
, Anisovich K.V.
, Shad M.S.
, Zhokhov S.S.
, Rybakov V.B.
, Dehaen W.
, Truhskov I.V.
, Ivanova O.А.
Oxidative cyclization of 5-aryl-1-benzyl-1,2,3-triazoles bearing electron-rich aromatic groups: ortho/ortho and ortho/ipso coupling
Chemistry of Heterocyclic Compounds. 2021.
V.57. N7-8. P.817-822. DOI: 10.1007/s10593-021-02985-5
WOS
Scopus
OpenAlex
|
|
45
|
Andreev I.A.
, Ratmanova N.K.
, Augustin A.U.
, Ivanova O.A.
, Levina I.I.
, Khrustalev V.N.
, Werz D.B.
, Trushkov I.V.
Protic Ionic Liquid as Reagent, Catalyst, and Solvent: 1‐Methylimidazolium Thiocyanate
Angewandte Chemie International Edition. 2021.
V.60. N14. P.7927-7934. DOI: 10.1002/anie.202016593
WOS
Scopus
OpenAlex
|
|
46
|
Vartanova A.E.
, Plodukhin A.Y.
, Ratmanova N.K.
, Andreev I.A.
, Anisimov M.N.
, Gudimchuk N.B.
, Rybakov V.B.
, Levina I.I.
, Ivanova O.A.
, Trushkov I.V.
, Alabugin I.V.
Expanding Stereoelectronic Limits of endo-tet Cyclizations: Synthesis of Benz[b]azepines from Donor–Acceptor Cyclopropanes
Journal of the American Chemical Society. 2021.
V.143. N34. P.13952-13961. DOI: 10.1021/jacs.1c07088
WOS
Scopus
OpenAlex
|
|
47
|
Vartanova A.E.
, Levina I.I.
, Rybakov V.B.
, Ivanova O.A.
, Trushkov I.V.
Donor–Acceptor Cyclopropane Ring Opening with 6-Amino-1,3-dimethyluracil and Its Use in Pyrimido[4,5-b]azepines Synthesis
Journal of Organic Chemistry. 2021.
V.86. N17. P.12300-12308. DOI: 10.1021/acs.joc.1c01064
WOS
Scopus
OpenAlex
|
|
48
|
Jacob A.
, Barkawitz P.
, Andreev I.A.
, Ratmanova N.K.
, Trushkov I.V.
, Werz D.B.
(3+2)-Cycloaddition of Donor–Acceptor Cyclopropanes with Thiocyanate: A Facile and Efficient Synthesis of 2-Amino-4,5-dihydrothiophenes
Synlett. 2021.
V.32. N09. P.901-904. DOI: 10.1055/a-1385-2385
WOS
Scopus
OpenAlex
|
|
49
|
Merkushev A.A.
, Makarov A.S.
, Shpuntov P.M.
, Abaev V.T.
, Trushkov I.V.
, Uchuskin M.G.
Oxidative Rearrangement of 2‐(2‐Aminobenzyl)furans: Synthesis of Functionalized Indoles and Carbazoles
European Journal of Organic Chemistry. 2021.
V.2021. N8. P.1274-1285. DOI: 10.1002/ejoc.202001608
WOS
Scopus
OpenAlex
|
|
50
|
Nguyen H.M.
, Chand H.R.
, Golantsov N.E.
, Trushkov I.V.
, Voskressensky L.G.
Cyclopentene Assembly by Microwave-Assisted Domino Reaction of Donor–Acceptor Cyclopropanes with Ketals
Synlett. 2020.
V.31. N03. P.295-299. DOI: 10.1055/s-0039-1690775
WOS
Scopus
OpenAlex
|
|
51
|
Kuznetsova L.I.
, Chagarovskiy A.O.
, Levina I.I.
, Rybakov V.B.
, Ivanova O.A.
, Trushkov I.V.
A simple synthesis of 2-{2-[(arylmethylidene)amino]-indazol-3-yl}malonate esters
Chemistry of Heterocyclic Compounds. 2020.
V.56. N5. P.555-561. DOI: 10.1007/s10593-020-02699-0
WOS
Scopus
OpenAlex
|
|
52
|
Boichenko M.A.
, Chagarovskiy A.O.
, Rybakov V.B.
, Trushkov I.V.
, Ivanova O.A.
Dimethyl 2-{[2-(2-Methoxy-1-methoxycarbonyl-2-oxoethyl)-4,5,7-trimethoxy-3-(2,4,5-trimethoxyphenyl)-2,3-dihydro-1H-inden-1-yl]methyl}malonate
Molbank. 2020.
V.2020. N1. M1107
. DOI: 10.3390/m1107
WOS
Scopus
OpenAlex
|
|
53
|
Chagarovskiy A.
, Ivanova O.
, Trushkov I.
Donor-acceptor cyclopropanes with nucleophilic group at ortho-position of donor aromatic substituent
Nucleation and Atmospheric Aerosols. 2020.
V.2280. N1. 050011
. DOI: 10.1063/5.0018466
Scopus
OpenAlex
|
|
54
|
Fadeev A.A.
, Chagarovskiy A.O.
, Makarov A.S.
, Levina I.I.
, Ivanova O.A.
, Uchuskin M.G.
, Trushkov I.V.
Synthesis of (Het)aryl 2-(2-hydroxyaryl)cyclopropyl Ketones
Molecules. 2020.
V.25. N23. 5748
. DOI: 10.3390/molecules25235748
WOS
Scopus
OpenAlex
|
|
55
|
Ratmanova N.K.
, Andreev I.A.
, Trushkov I.V.
Methods for the synthesis of immunostimulant plerixafor
Chemistry of Heterocyclic Compounds. 2020.
V.56. N1. P.30-35. DOI: 10.1007/s10593-020-02617-4
WOS
Scopus
OpenAlex
|
|
56
|
Ratmanova N.K.
, Andreev I.A.
, Leontiev A.V.
, Momotova D.
, Novoselov A.M.
, Ivanova O.A.
, Trushkov I.V.
Strategic approaches to the synthesis of pyrrolizidine and indolizidine alkaloids
Tetrahedron. 2020.
V.76. N14. 131031
. DOI: 10.1016/j.tet.2020.131031
WOS
Scopus
OpenAlex
|
|
57
|
Zelina E.Y.
, Nevolina T.A.
, Sorotskaja L.N.
, Skvortsov D.A.
, Trushkov I.V.
, Uchuskin M.G.
Route to pyrrolo[1,2-a]quinoxalines via a furan ring opening-pyrrole ring closure sequence
Tetrahedron Letters. 2020.
V.61. N9. 151532
. DOI: 10.1016/j.tetlet.2019.151532
WOS
Scopus
OpenAlex
|
|
58
|
Boichenko M.A.
, Andreev I.A.
, Chagarovskiy A.O.
, Levina I.I.
, Zhokhov S.S.
, Trushkov I.V.
, Ivanova O.A.
Ring Opening of Donor–Acceptor Cyclopropanes with Cyanide Ion and Its Surrogates
Journal of Organic Chemistry. 2020.
V.85. N2. P.1146-1157. DOI: 10.1021/acs.joc.9b03098
WOS
Scopus
OpenAlex
|
|
59
|
Trushkov I.V.
, Uchuskin M.G.
, Abaev V.T.
, Serdyuk O.V.
Indolylvinyl Ketones: Building Blocks for the Synthesis of Natural Products and Bioactive Compounds
Synthesis-Stuttgart. 2019.
V.51. N04. P.787-815. DOI: 10.1055/s-0037-1611702
WOS
Scopus
OpenAlex
|
|
60
|
Chagarovskiy A.O.
, Kuznetsov V.V.
, Ivanova O.A.
, Goloveshkin A.S.
, Levina I.I.
, Makhova N.N.
, Trushkov I.V.
Synthesis of 1‐Substituted Pyrazolines by Reaction of Donor‐Acceptor Cyclopropanes with 1,5‐Diazabicyclo[3.1.0]hexanes
European Journal of Organic Chemistry. 2019.
V.2019. N31-32. P.5475-5485. DOI: 10.1002/ejoc.201900579
WOS
Scopus
OpenAlex
|