Novel approach to the design of potential bioactive alkaloid anabasine conjugates using click chemistry methodology
Anabasine‐containing azides and acetylenes were used as building blocks in copper(I)‐catalyzed 1,3‐dipolar cycloaddition reactions with a series of acetylenes and azides via click methodology to provide a range of anabasine conjugates being potential ligands for neuronal nicotinic acetylcholine rece...
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| Veröffentlicht in: | Heteroatom chemistry 2016-09, Vol.27 (5), p.245-252 |
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| container_end_page | 252 |
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| container_issue | 5 |
| container_start_page | 245 |
| container_title | Heteroatom chemistry |
| container_volume | 27 |
| creator | Artyushin, Oleg I. Vinogradova, Natalya M. Sharova, Elena V. Genkina, Galina K. Brel, Valery K. |
| description | Anabasine‐containing azides and acetylenes were used as building blocks in copper(I)‐catalyzed 1,3‐dipolar cycloaddition reactions with a series of acetylenes and azides via click methodology to provide a range of anabasine conjugates being potential ligands for neuronal nicotinic acetylcholine receptors. |
| doi_str_mv | 10.1002/hc.21322 |
| format | Article |
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| language | eng |
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| source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
| title | Novel approach to the design of potential bioactive alkaloid anabasine conjugates using click chemistry methodology |
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