Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/131163
Title: 4-Hydroxy-2-pyrones: Synthesis, Natural Products, and Application
Authors: Fedin, V. V.
Obydennov, D. L.
Usachev, S. A.
Sosnovskikh, V. Y.
Issue Date: 2023
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
Citation: Fedin, V, Obydennov, D, Usachev, S & Sosnovskikh, V 2023, '4-Hydroxy-2-pyrones: Synthesis, Natural Products, and Application', Organics, Том. 4, № 4, стр. 539-561. https://doi.org/10.3390/org4040037
Fedin, V., Obydennov, D., Usachev, S., & Sosnovskikh, V. (2023). 4-Hydroxy-2-pyrones: Synthesis, Natural Products, and Application. Organics, 4(4), 539-561. https://doi.org/10.3390/org4040037
Abstract: 4-Hydroxy-2-pyrones are of interest as potential biorenewable molecules for a sustainable transition from biomass feedstock to valuable chemical products. This review focuses on the methodologies for the synthesis of 4-hydroxy-2-pyrones published over the last 20 years. These pyrones as polyketides are widespread in Nature and possess versatile bioactivity that makes them an attractive target for synthesis and modification. Biosynthetic paths of the pyrones are actively developed and used as biotechnological approaches for the construction of natural and unnatural polysubstituted 4-hydroxy-2-pyrones. The major synthetical methods are biomimetic and are based on the cyclization of tricarbonyl compounds. Novel chemical methods of de novo synthesis based on alkyne cyclizations using transition metal complexes and ketene transformations allow for straightforward access to 4-hydroxy-2-pyrones and have been applied for the construction of natural products. Possible directions for further pyrone ring modification are discussed. © 2023 by the authors.
Keywords: 2-PYRONE
4-HYDROXY-2-PYRONE
4-PYRONE
BIOLOGICAL ACTIVITY
CYCLIZATION
KETENE
KETOACETYLENE
NATURAL PRODUCTS
POLYKETIDE
TRIACETIC ACID LACTONE
URI: http://elar.urfu.ru/handle/10995/131163
Access: info:eu-repo/semantics/openAccess
cc-by
License text: https://creativecommons.org/licenses/by/4.0/
SCOPUS ID: 85185691563
WOS ID: 001130919800001
PURE ID: 51667625
ISSN: 2673-401X
DOI: 10.3390/org4040037
Sponsorship: Russian Science Foundation, RSF: 22-73-10236
This work was financially supported by the Russian Science Foundation (grant 22-73-10236, https://rscf.ru/project/22-73-10236/(accessed on 10 December 2023)).
RSCF project card: 22-73-10236
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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