Alexey Festa

Dr. Alexey Festa

RUDN University
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 July 2019 in Chemical Society Reviews
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AFAlexey Festa
Alexey Festa
LVLeonid G. Voskressensky
Leonid G. Voskressensky
EEErik Van Der Eycken
Erik Van Der Eycken
The impact of visible light-promoted chemistry on the functionalization of indoles and related heterocycles is reviewed.

1 July 2024 in Russian Chemical Reviews
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Journal Article
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Valery N. CharushinValery N. Charushin
Valery N. Charushin
EVEgor Verbitskiy
Egor Verbitskiy
OCOleg N. Chupakhin
Oleg N. Chupakhin
DVD. V. Vorobyeva
D. V. Vorobyeva
PGPavel S. Gribanov
Pavel S. Gribanov
Alexey Yu. FedorovAlexey Yu. Fedorov
Alexey Yu. Fedorov
The chemistry of heterocyclic compounds has traditionally been and remains a bright area of chemical science in Russia. This is due to the fact that many heterocycles find the widest application. These compounds are the key structural fragments of most drugs, plant protection agents. Many natural compounds are also derivatives of heterocycles. At present, more than half of the hundreds of millions of known chemical compounds are heterocycles. This collective review is devoted to the achievements of Russian chemists in this field over the last 15–20 years. The review presents the achievements of leading heterocyclists representing both RAS institutes and university science. It is worth noting the wide scope of the review, both in terms of the geography of author teams, covering the whole of our large country, and in terms of the diversity of research areas. Practically all major types of heterocycles are represented in the review. The special attention is focused on the practical applications of heterocycles in the design of new drugs and biologically active compounds, high-energy molecules, materials for organic electronics and photovoltaics, new ligands for coordination chemistry, and many other rapidly developing areas. These practical advances would not be possible without the development of new fundamental transformations in heterocyclic chemistry. Bibliography — 2237 references.

17 November 2023 in Chemical Society Reviews
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AFAlexey Festa
Alexey Festa
OSOlga A. Storozhenko
Olga A. Storozhenko
LVLeonid G. Voskressensky
Leonid G. Voskressensky
EEErik Van Der Eycken
Erik Van Der Eycken
The use of visible light and photoredox catalysis emerged as a powerful and sustainable tool for organic synthesis, showing high value for distinctly different ways of bond creation. Halogenated compounds are the cornerstone of contemporary organic synthesis: it is almost impossible to develop a route towards a pharmaceutical reagent, agrochemical, natural product, etc. without the involvement of halogen-containing intermediates. Moreover, the halogenated derivatives as final products became indispensable for drug discovery and materials science. The idea of this review is to understand and summarise the impact of visible light-promoted chemistry on halogenation and halofunctionalisation reactions.


24 December 2019 in The Journal of Organic Chemistry
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Journal Article
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OSOlga A. Storozhenko
Olga A. Storozhenko
AFAlexey Festa
Alexey Festa
GDGalina I. Detistova
Galina I. Detistova
VRVictor B. Rybakov
Victor B. Rybakov
AVAlexey V. Varlamov
Alexey V. Varlamov
LVLeonid G. Voskressensky
Leonid G. Voskressensky

13 September 2021 in Molecules
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RARajeshwar Reddy Aleti
Rajeshwar Reddy Aleti
AFAlexey Festa
Alexey Festa
LVLeonid G. Voskressensky
Leonid G. Voskressensky
EEErik Van Der Eycken
Erik Van Der Eycken
Phenanthridinones are important heterocyclic frameworks present in a variety of complex natural products, pharmaceuticals and displaying wide range of pharmacological actions. Its structural importance has evoked a great deal of interest in the domains of organic synthesis and medicinal chemistry to develop new synthetic methodologies, as well as novel compounds of pharmaceutical interest. This review focuses on the synthesis of phenanthridinone scaffolds by employing aryl-aryl, N-aryl, and biaryl coupling reactions, decarboxylative amidations, and photocatalyzed reactions.