Synthesis of linear hetarenochromones based on 7-hydroxy-6-formyl(acetyl)chromones
Тип публікації :
Стаття
Дата випуску :
2021
Автор(и) :
Shokol, Tatyana
Natalia, Gorbulenko
Volodymyr, Khilya
Мова основного тексту :
Англійська
eKNUTSHIR URL :
Том :
9
Випуск :
1
ISSN :
2312-3222
Початкова сторінка :
70
Кінцева сторінка :
96
Цитування :
[APA 7] Shokol, T., Natalia, G., & Volodymyr, K. (2021). Synthesis of linear hetarenochromones based on 7-hydroxy-6-formyl(acetyl)chromones. French-Ukrainian Journal of Chemistry, 9(1), 70–96. https://doi.org/10.17721/fujcV9I1P70-96
[ДСТУ] Shokol T., Natalia G., Volodymyr K. Synthesis of linear hetarenochromones based on 7-hydroxy-6-formyl(acetyl)chromones. French-Ukrainian Journal of Chemistry. 2021. Vol. 9, no. 1. P. 70—96. DOI: 10.17721/fujcV9I1P70-96 (date of access: 25.07.2026).
Fused chromones are attracting increasing attention as novel therapeutic agents due to their wide distribution in nature, effective bioactivities and low toxicity. 6-Carbonyl-7-hydroxychromones proved to be versatile synthons for the synthesis of linear hetarenochromones by annulation of heterocycle to the chromone core. The present review is focused on the syntheses of furo[3,2-g]chromones, pyrano[3,2-g]chromones and some of their N-containing analogues, namely chromeno[6,7-d]isoxazoles, pyrano[3’,2’:6,7]chromeno[4,3-b]pyridine-5,11-diones and pyrano[3’,2’:6,7]chromeno[4,3-c]pyridine-5,11-diones based on the 7-hydroxy-6-formylchromones or 7-hydroxy-6-acetylchromones and shows the current state of research to date. The methods for the synthesis of the starting 7-hydroxy-6-formylchromones and 7-hydroxy-6-acetylchromones have been also mentioned. The biological activity of naturally occurring and modified synthetic linear hetarenochromones has been also represented.
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