A tunable copper-catalyzed multicomponent reaction towards alkaloid-inspired indole/lactam polycycles
A versatile copper(i)-catalyzed cascade multicomponent reaction strategy between readily available (Z)-3-iodoacrylic acids, terminal alkynes, and primary amines is reported, leading to a great diversity of complex heterocyclic backbones based on biorelevant indole/lactam scaffolds.
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Veröffentlicht in: | Organic & biomolecular chemistry 2017-04, Vol.15 (15), p.3304-3309 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A versatile copper(i)-catalyzed cascade multicomponent reaction strategy between readily available (Z)-3-iodoacrylic acids, terminal alkynes, and primary amines is reported, leading to a great diversity of complex heterocyclic backbones based on biorelevant indole/lactam scaffolds. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c7ob00532f |