Maxim E. Kukushkin - Concepedia

Author

Maxim E. Kukushkin

Lomonosov Moscow State University ORCID

Also Known As

Kukushkin, Maxim E., M. E. Kukushkin, Maxim E. Kukushkin, Maxim E Kukushkin, Maxim E. Kukushkin

Publications

373

Citations

H-Index

Concepts

All Affiliations

Lomonosov Moscow State University National University of Science and Technology D. Mendeleyev University of Chemical Technology of Russia Peoples' Friendship University of Russia Skolkovo Institute of Science and Technology

About

Maxim E. Kukushkin is an author at Lomonosov Moscow State University specializing in biomolecular engineering, chemistry, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biomolecular Engineering	5	5	231
2	Engineering	3	3	185
3	Natural Sciences	3	3	179
4	Biochemistry	2	2	37
5	Medicine	1	1	14

Maxim E. Kukushkin

Publications

334

Citations

H-Index

Page 1

	Year	Citations
The chemistry of heterocycles in the 21st century Valery N. Charushin, Egor V. Verbitskiy, Daria V. Vorobyeva, Russian Chemical Reviews Medicinal ChemistryDiversity Oriented SynthesisEngineeringHeterocyclicNatural Sciences	2024	142
Synthesis, isomerization and biological activity of novel 2-selenohydantoin derivatives Yan A. Ivanenkov, Mark S. Veselov, Igor G. Rezekin, Bioorganic & Medicinal Chemistry Novel 2-Selenohydantoin DerivativesNatural Product SynthesisDerivative (Chemistry)Synthetic ChemistryBiomolecular Engineering	2016	32
Dispirooxindoles Based on 2-Selenoxo-Imidazolidin-4-Ones: Synthesis, Cytotoxicity and ROS Generation Ability Vladimir Novotortsev, Maxim E. Kukushkin, Dmitry A. Skvortsov, International Journal of Molecular Sciences	2021	24
Regioselective Cycloaddition of Nitrile Imines to 5-Methylidene-3-phenyl-hydantoin: Synthesis and DFT Calculations Maria E. Filkina, Daria N. Baray, Yuri K. Grishin, International Journal of Molecular Sciences Combinatorial ChemistryEngineeringHeterocyclicBiochemistryNatural Sciences	2023	23
Diffusion mixing with a volatile tertiary amine as a very efficient technique for 1,3-dipolar cycloaddition reactions proceeding <i>via</i> dehydrohalogenation of stable precursors of reactive dipoles Dmitry E. Shybanov, Maria E. Filkina, Maxim E. Kukushkin, New Journal of Chemistry Tertiary Amine VaporsNitrilimine GenerationEngineeringHeterocyclicStable Precursors	2022	20
Synthesis and Biological Evaluation of Novel Dispiro-Indolinones with Anticancer Activity Yan A. Ivanenkov, Maxim E. Kukushkin, Anastasia A. Beloglazkina, Molecules	2023	19
[3+2]-Cycloaddition of Nitrile Imines to Parabanic Acid Derivatives—An Approach to Novel Spiroimidazolidinediones Juliana Kuznetsova, Varvara T. Tkachenko, Lada M. Petrovskaya, International Journal of Molecular Sciences	2023	17
Synthesis and cytotoxicity of oxindoles dispiro derivatives with thiohydantoin and adamantane fragments Maxim E. Kukushkin, Dmitriy A. Skvortsov, Marina Kalinina, Phosphorus, sulfur, and silicon and the related elements Organic ChemistryChemistrySignificant P53 ActivationReporter ConstructionHeterocycle Chemistry	2020	14
[4+2]-Cycloaddition to 5-Methylidene-Hydantoins and 5-Methylidene-2-Thiohydantoins in the Synthesis of Spiro-2-Chalcogenimidazolones Dmitry E. Shybanov, Maxim E. Kukushkin, Yanislav S. Hrytseniuk, International Journal of Molecular Sciences	2023	12
A convenient synthesis of 3-aryl-5-methylidene-2-thiohydantoins Maxim E. Kukushkin, Dmitry E. Shybanov, N. V. Zyk Mendeleev Communications	2022	11

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