V
Vladimir V. Zarubaev
Researcher at Pasteur Institute
Publications - 142
Citations - 1902
Vladimir V. Zarubaev is an academic researcher from Pasteur Institute. The author has contributed to research in topics: Virus & Chemistry. The author has an hindex of 19, co-authored 110 publications receiving 1356 citations.
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Journal ArticleDOI
First example of the cascade acylation/IMDAV/ene reaction sequence, leading to N-arylbenzo[f]isoindole-4-carboxylic acids possessing anti-viral activity
Alexander A. Voronov,Kseniia A. Alekseeva,Elena A. Ryzhkova,Vladimir V. Zarubaev,Anastasia V. Galochkina,Vladimir P. Zaytsev,Mahesh S. Majik,Santosh G. Tilve,Atash V. Gurbanov,Atash V. Gurbanov,Fedor I. Zubkov +10 more
TL;DR: The reaction between readily accessible N-aryl-3-phenylally-lamines and maleic anhydride led to unexpected products -polysubstituted hydrogenated benzo[f]isoindole-4-carboxylic acids as discussed by the authors.
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The Evolution of Pleconaril: Modified O-Alkyl Linker Analogs Have Biological Activity towards Coxsackievirus B3 Nancy.
Alexandrina S. Volobueva,Anna Egorova,Anastasia V. Galochkina,Sean Ekins,Vladimir V. Zarubaev,Vadim Makarov +5 more
TL;DR: The core-structure of pleconaril, a well-known antienteroviral drug candidate, is used for the synthesis of novel compounds with O-propyl linker modifications that exhibited a strong anti-CVB3 activity.
Journal Article
In vitro and in vivo effects of ingavirin on the ultrastructure and infectivity of influenza virus
Vladimir V. Zarubaev,Beliaevskaia Sv,Sirotkin Ak,Pavel Anfimov,Nebol'sin Ve,Oleg I. Kiselev,Reĭkhart Dv +6 more
TL;DR: The findings suggest that Ingavirin is able to impair the processes of viral morphogenesis, which in turn leads to a reduction in the infectivity of progeny virions.
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The 1,3-dipolar cycloaddition of adamantine-derived nitrones with maleimides
Alexander P. Molchanov,Valentina M. Lukina,Mariia M. Efremova,Anna A. Muryleva,Alexander V. Slita,Vladimir V. Zarubaev +5 more
TL;DR: Adamantane-derived aldo- and ketonitrones react with maleimides giving corresponding isoxazolidines as discussed by the authors, and in the case of aldonitrones reactions proceed giving the diastereomeric mixtures.
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Water-Promoted Reaction of C60Ar5Cl Compounds with Thiophenes Delivers a Family of Multifunctional Fullerene Derivatives with Selective Antiviral Properties.
Olga A. Kraevaya,Valeriya S. Bolshakova,Alexander S. Peregudov,Alexander V. Chernyak,Nikita A. Slesarenko,Vitaliy Yu. Markov,Natalia S. Lukonina,Vyacheslav M. Martynenko,Ekaterina O. Sinegubova,Alexander F. Shestakov,Vladimir V. Zarubaev,Dominique Schols,Pavel A. Troshin +12 more
TL;DR: In this paper, a reaction of the fullerene derivatives C60Ar5Cl was reported, which enables the substitution of Cl with thiophene residues and the formation of the novel family of C1-symmetrical C60 derivatives with six functional addends.