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Maxim G. Uchuskin
Observed names:
M. G. Uchuskin,
Maxim G Uchuskin,
Maxim Uchuskin,
Uchuskin, Maxim,
Uchuskin, Maxim G,
Uchuskin, Maxim G.
show all 6
Institutions:
Perm State University,
Institute of Technical Chemistry,
Ural Branch of the Russian Academy of Sciences
Observed institutions:
Perm State University,
Peoples' Friendship University of Russia,
Southern Federal University,
Kuban State Technological University,
North Ossetian State University,
Institute of Technical Chemistry,
Ural Branch of the Russian Academy of Sciences
show all 7
ORCID:
0000-0001-9008-7610
Observed ORCID:
0000-0001-9008-7610
OpenAlex ID:
A5062361390
Furan Oxidation Reactions in the Total Synthesis of Natural Products
2018
·
Maxim Uchuskin
, Igor Trushkov
, et al.
·
Synthesis
·
81
From biomass to medicines. A simple synthesis of indolo[3,2-c]quinolines, antimalarial alkaloid isocryptolepine, and its derivatives
2012
·
Maxim G. Uchuskin
, Arkady S. Pilipenko
, et al.
·
Organic & Biomolecular Chemistry
·
68
Furan's Gambit: Electrophile‐Attack‐Triggered Sacrifice of Furan Rings for the Intramolecular Construction of Azaheterocycles
2015
·
Igor V. Trushkov
, Maxim G. Uchuskin
, et al.
·
European Journal of Organic Chemistry
·
60
A Simple Route to Polysubstituted Indoles Exploiting Azide Induced Furan Ring Opening
2014
·
Vladimir T. Abaev
, Anastasiya T. Plieva
, et al.
·
Organic Letters
·
46
Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues
2016
·
Anton S. Makarov
, Anton A. Merkushev
, et al.
·
Organic Letters
·
37
Furan ring opening–indole ring closure: SnCl2-induced reductive transformation of difuryl(2-nitroaryl)methanes into 2-(2-acylvinyl)indoles
2012
·
Maxim G. Uchuskin
, Natalia V. Molodtsova
, et al.
·
Tetrahedron
·
35
Intramolecular azavinyl carbene-triggered rearrangement of furans
2019
·
Anton S. Makarov
, Maxim G. Uchuskin
, et al.
·
Chemical Science
·
28
PDF
Furan Ring‐Opening/Indole Ring‐Closure: Pictet–Spengler‐Like Reaction of 2‐(o‐Aminophenyl)furans with Aldehydes
2010
·
Alexander V. Butin
, Maxim G. Uchuskin
, et al.
·
European Journal of Organic Chemistry
·
26
Synthesis, Antimicrobial and Antibiofilm Activities, and Molecular Docking Investigations of 2-(1H-Indol-3-yl)-1H-benzo[d]imidazole Derivatives
2023
·
Elena Y. Mendogralo
, Larisa Y. Nesterova
, et al.
·
Molecules
·
25
PDF
The Butin reaction
2016
·
Vladimir T. Abaev
, Igor V. Trushkov
, et al.
·
Chemistry of Heterocyclic Compounds
·
25
Indolylvinyl Ketones: Building Blocks for the Synthesis of Natural Products and Bioactive Compounds
2019
·
Olga Serdyuk
, Igor Trushkov
, et al.
·
Synthesis
·
23
A Route to (Het)arene-Annulated Pyrrolo[1,2- d ][1,4]diazepines via the Expanded Intramolecular Paal–Knorr Reaction: Nitro Group and Furan Ring as Equivalents of Amino Group and 1,4-Diketone
2019
·
Elena Y. Zelina
, Tatyana A. Nevolina
, et al.
·
The Journal of Organic Chemistry
·
22
Extended Version of the Corey–Chaykovsky Reaction: Synthesis of 2,4-Substituted Furans by the Treatment of β-Dialkylamino Chalcones with Dimethylsulfonium Methylide
2023
·
Roman O. Shcherbakov
, Danil A. Myasnikov
, et al.
·
The Journal of Organic Chemistry
·
19
Extended Corey–Chaykovsky reactions: transformation of 2-hydroxychalcones to benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans
2021
·
Alexander A. Fadeev
, Anton S. Makarov
, et al.
·
Organic Chemistry Frontiers
·
19
Intramolecular Palladium-Catalyzed Oxidative Amination of Furans: Synthesis of Functionalized Indoles
2018
·
Anton S. Makarov
, Maxim G. Uchuskin
, et al.
·
The Journal of Organic Chemistry
·
19
A General Synthetic Route to Isomeric Pyrrolo[1,2-x][1,4]diazepinones
2018
·
Elena Y. Zelina
, Tatyana A. Nevolina
, et al.
·
The Journal of Organic Chemistry
·
19
Synthesis of Indoles by Domino Reaction of 2‐(Tosylamino)benzyl Alcohols with Furfurylamines: Two Opposite Reactivity Modes of the α‐Carbon of the Furan Ring in One Process
2014
·
Maxim G. Uchuskin
, Natalia V. Molodtsova
, et al.
·
European Journal of Organic Chemistry
·
19
A Simple Synthesis of Densely Substituted Benzofurans by Domino Reaction of 2-Hydroxybenzyl Alcohols with 2-Substituted Furans
2019
·
Anton S. Makarov
, Anna E. Kekhvaeva
, et al.
·
Synthesis
·
18
Recyclization of (2-Aminophenyl)bis(5-tert-butyl-2-furyl)methanes into Indole Derivatives: Unusual Dependence on Substituent at Nitrogen Atom
2008
·
Alexander Butin
, Sergey Smirnov
, et al.
·
Synthesis
·
18
Intramolecular iron-catalyzed transannulation of furans with O -acetyl oximes: synthesis of functionalized pyrroles
2021
·
Anton S. Makarov
, Alexander A. Fadeev
, et al.
·
Organic Chemistry Frontiers
·
17
Furan Ring Opening - Pyridine Ring Closure: New Route to Quinolines under the Bischler-Napieralski Reaction Conditions
2011
·
Alexander Butin
, Fatima Tsiunchik
, et al.
·
Synthesis
·
17
Furan Ring Opening-Pyrrole Ring Closure: Simple Route to 5-Alkyl-2-(aminomethyl)pyrroles
2010
·
Alexander Butin
, Tatyana Nevolina
, et al.
·
Synthesis
·
16
Converting Strain Release into Aromaticity Loss for Activation of Donor–Acceptor Cyclopropanes: Generation of Quinone Methide Traps for C-Nucleophiles
2024
·
Vitaly V. Shorokhov
, Beauty K. Chabuka
, et al.
·
Organic Letters
·
14
The Synthesis and Biological Evaluation of 2-(1H-Indol-3-yl)quinazolin-4(3H)-One Derivatives
2023
·
Elena Y. Mendogralo
, Larisa Y. Nesterova
, et al.
·
Molecules
·
14
PDF
CuBr2-catalyzed alkylation of furans with benzyl alcohols and benzaldehydes. Domino reactions including this alkylation as a key step
2017
·
Anton S. Makarov
, Anna E. Kekhvaeva
, et al.
·
Tetrahedron
·
14
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Works count:
105
Citation count:
900
H-index:
18
I10-index:
32
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