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ИССЛЕДОВАТЕЛЬСКАЯ
ЛАБОРАТОРИЯ
Органического синтеза
Two Faces of Styrylsulfonium Salts: Domino Michael Addition/Cyclopropanation of 2-(2-Acylvinyl)indoles for the Synthesis of Cyclopropa[3,4]pyrrolo[1,2-a]indoles
Alexander A. Fedorov, Danil A. Myasnikov, Elena Y. Mendogralo, Igor V. Trushkov, and Maxim G. Uchuskin. The Journal of Organic Chemistry 2025 90 (7), 2682-2687
Oxidative Transformation of 2-Furylanilines into Indolin-3-ones
Ekaterina R. Nasibullina, Elena Y. Mendogralo, Anton A. Merkushev, Anton S. Makarov, and Maxim G. Uchuskin. J. Org. Chem. 2024, 89, 9, 6602–6606
Unveiling Orthogonal Reactivity of Substituted 2-(2-Azidostyryl)furans: Thermolysis and Photolysis versus Catalysis
Yury A. Vasev, Ekaterina R. Nasibullina, Anton S. Makarov, and Maxim G. Uchuskin. Org. Lett. 2023, 25, 43, 7780–7785
Mechanistic Insight into Palladium-Catalyzed Asymmetric Alkylation of Indoles with Diazoesters Employing Bipyridine-N,N’-dioxides as Chiral Controllers
Yasuaki Fukazawa, Vladimir Yu. Vaganov, Julia V. Burykina, Artem N. Fakhrutdinov, Ruslan I. Safiullin, Felix Plasser, Aleksandr E. Rubtsov, Valentine P. Ananikov, Andrei V. Malkov. Advanced Synthesis & Catalysis. Volume 366, Issue 1. p. 121-133
Interrupted Furan–Yne Cyclization: Access to Unsaturated Dicarbonyl Compounds and Their Subsequent Transformation into Functionalized Pyridazines
Yury A. Vasev, Ekaterina R. Nasibullina, Anton S. Makarov, and Maxim G. Uchuskin. Org. Lett. 2023, 25, 43, 7780–7785
Synthesis of tetrahydrofuro[3,2-c]pyridines via Pictet–Spengler reaction
Elena Y. Mendogralo and Maxim G. Uchuskin. Beilstein J. Org. Chem. 2023, 19, 991–997
De novo three-component synthesis of meta-substituted anilines
Anton S. Makarov, Arthur N. Bakiev and Diana A. Eshmemeteva. Org. Chem. Front., 2023,10, 2760-2765
Synthetic strategy toward push-pull chromophores on furan-, benzofuran-, pyrrole-, and indole-based matrices
Danil K. Vshivkov, Arthur N. Bakiev, Diana A. Eshmemeteva, Anton S. Makarov
Extended Version of the Corey–Chaykovsky Reaction: Synthesis of 2,4-Substituted Furans by the Treatment of β-Dialkylamino Chalcones with Dimethylsulfonium Methylide
Roman O. Shcherbakov, Danil A. Myasnikov, Igor V. Trushkov, and Maxim G. Uchuskin. Cite this: J. Org. Chem. 2023, 88, 13, 8227–8235
Short Electrochemical Asymmetric Synthesis of (+)-N-Acetylcolchinol
Yi Du, Adelaide Lunga, Aleksandr E. Rubtsov and Andrei V. Malkov.
Green Chemistry. 01 Sep 2022.
Green Chemistry. 01 Sep 2022.
One-Step Synthesis of Triphenylphosphonium Salts from (Het)arylmethyl Alcohols
Petrakis N. Chalikidi, Taimuraz T. Magkoev, Andrey V. Gutnov, Oleg P. Demidov, Maxim G. Uchuskin, Igor V. Trushkov, Vladimir T. Abaev. Cite this: J. Org. Chem. 2021, 86, 14, 9838–9846
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
Roman O. Shcherbakov, Diana A. Eshmemet’eva, Anton A. Merkushev, Igor V. Trushkov, Maxim G. Uchuskin. Molecules. 2021 May; 26(9): 2637.
Oxidative Rearrangement of 2-(2-Aminobenzyl)furans: Synthesis of Functionalized Indoles and Carbazoles
Anton A. Merkushev, Anton S. Makarov, Pavel M. Shpuntov, Vladimir T. Abaev, Igor V. Trushkov, Maxim G. Uchuskin. European Journal of Organic Chemistry 2021(8)
A synthetic diterpene analogue inhibits mycobacterial persistence and biofilm formation by targeting (p)ppGpp synthetases
Alexander G Tkachenko, Natalya M Kashevarova, Roman Yu Sidorov, Larisa Yu Nesterova, Anna V Akhova, Ivan V Tsyganov, Vladimir Yu Vaganov, Sergei A Shipilovskikh, Aleksandr E Rubtsov, Andrei V Malkov. Cell Chem Biol. 2021 Feb 9
Developing a Methodology for Catalytic Asymmetric Crotylation of Aldehydes
Aleksandr E. Rubtsov, Andrei V. Malkov. 2021. Synlett
Recent Advances in the Synthesis of 2,2′-Bipyridines and Their Derivatives
Aleksandr E. Rubtsov, Andrei V. Malkov. 2021. Synthesis (Germany)
Oxidative Rearrangement of 2‐(2‐Aminobenzyl)furans: Synthesis of Functionalized Indoles and Carbazoles
Dr. Anton A. Merkushev Dr. Anton S. Makarov Pavel M. Shpuntov Prof. Dr. Vladimir T. Abaev Prof. Dr. Igor V. Trushkov Dr. Maxim G. Uchuskin. European Journal of Organic Chemistry. Volume 2021, Issue 8, 25 February 2021, Pages 1274-1285
A Mild Method for Electrochemical Reduction of Heterocyclic N‐Oxides
Fukazawa, Y., Rubtsov, A.E., Malkov, A.V. (2020) European Journal of Organic Chemistry, 2020 (22), pp. 3317-3319.
Optimization of Catalyst Structure for Asymmetric Propargylation of Aldehydes with Allenyltrichlorosilane
Vaganov, V.Y., Fukazawa, Y., Kondratyev, N.S., Rubtsov, A.E., Malkov, A.V. Advanced Synthesis and Catalysis, 2020, 362(23), стр. 5467–5474
Recyclization of 3-(Thiophen-2-yl)imino-3H-furan-2-ones under the Action of Cyanoacetic Acid Derivatives
Shipilovskikh, S.A., Rubtsov, A.E. Russian Journal of General Chemistry, 2020, 90(5), стр. 809–814
Route to pyrrolo[1,2-a]quinoxalines via a furan ring opening-pyrrole ring closure sequence
Zelina, E.Y., Nevolina, T.A., Sorotskaja, L.N., ...Trushkov, I.V., Uchuskin, M.G. Tetrahedron Letters, 2020, 61(9), 151532
Synthesis and Antinociceptive Activity of N-Substituted 4-Aryl-4-oxo-2-[(3-thiophen-2-yl)amino]but-2-enamides
Shipilovskikh, S.A., Vaganov, V.Y., Makhmudov, R.R., Rubtsov, A.E. Russian Journal of General Chemistry, 2020, 90(4), стр. 583–589
Synthesis of (Het)aryl 2-(2-hydroxyaryl)cyclopropyl Ketones
Fadeev, A.A., Chagarovskiy, A.O., Makarov, A.S., Uchuskin, M.G., Trushkov, I.V. Molecules (Basel, Switzerland), 2020, 25(23)
Synthesis of New Substituted 3-(Thien-2-yl)imino-3H-furan-2-ones
Shipilovskikh, S.A., Rubtsov, A.E. Russian Journal of General Chemistry, 2020, 90(6), стр. 943–947
