Please use this identifier to cite or link to this item:
https://elib.belstu.by/handle/123456789/48623
Title: | Synthesis of Novel 1,2,6-Trisubstituted Indoles Based on Cyclohexenone Scaffold |
Authors: | Arol, A. S. Mikhalyonok, S. G. Bezborodov, V. S. Kuz’menok, N. M. Savelyeu, A.I. |
Keywords: | heterocyclic systems гетероциклические системы indoles индолы ketones кетоны amines амины |
Issue Date: | 2021 |
Citation: | Synthesis of Novel 1,2,6-Trisubstituted Indoles Based on Cyclohexenone Scaffold / A. S. Arol [et. al.] // Современные проблемы органической химии : тезисы докладов Всероссийской научной конференции с международным участием, посвященная 90-летию со дня рождения академика В. Н. Коптюга, 9-11 июня 2021 г., Новосибирск. - Новосибирск, 2021. - С. 101. |
Abstract: | New methods of construction of heterocyclic systems are always attracting the interest from organic and medicinal chemists because such substances have significant potential in drug discovery. In this field indoles synthesis occupies a prominent place because of the high biological activity of indoles derivatives. The transformation of γ,δ-unsaturated ketones represents a good method for making pyrrole and indole core. In our work we focused on creating of indole core based on cyclohex-2-enone scaffold. |
URI: | https://elib.belstu.by/handle/123456789/48623 |
Appears in Collections: | Публикации в зарубежных изданиях |
Files in This Item:
File | Description | Size | Format | |
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Arol_Synthesis.pdf | 332.57 kB | Adobe PDF | View/Open |
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