The synthesis of angular heteroarenochromones based on 7-hydroxy-8-carbonylchromones

Тип публікації :
Стаття
Дата випуску :
2017
Автор(и) :
Shokol, Tatyana
Lozinski, Oleg
Gorbulenko, Natalia
Khilya, Volodymyr
Мова основного тексту :
Англійська
eKNUTSHIR URL :
DOI :
Журнал :
Том :
5
Випуск :
2
ISSN :
2312-3222
Початкова сторінка :
68
Кінцева сторінка :
94
Цитування :
[APA 7] Shokol, T., Lozinski, O., Gorbulenko, N., & Khilya, V. (2017). The synthesis of angular heteroarenochromones based on 7-hydroxy-8-carbonylchromones. French-Ukrainian Journal of Chemistry, 5(2), 68–94. https://doi.org/10.17721/fujcV5I2P68-94
[ДСТУ] The synthesis of angular heteroarenochromones based on 7-hydroxy-8-carbonylchromones / T. Shokol et al. French-Ukrainian Journal of Chemistry. 2017. Vol. 5, no. 2. P. 68—94. DOI: 10.17721/fujcV5I2P68-94 (date of access: 18.07.2026).
The present review highlights advanced strategies to the synthesis of the chromones annulated with O- and N-containing heterocycles at C(7)-C(8) bond. Due to the prevalence of such motives in different kinds of natural flavonoids and some alkaloids, fused chromones have attracted a great deal of attention so far. On the other hand a wide range of biological activities is displayed by the compounds of this type both among naturally occurring flavonoids and their synthetic analogues. 8-Carbonyl-7-hydroxychromones proved to be versatile synthones for the synthesis of angular hetarenochromones via approach of annulation of a heterocycle to the chromone core. It also addresses the question of the biological activity of naturally occurring and fused synthetic hetarenochromones.
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