Highly Efficient CuBr-Catalyzed Cross-Dehydrogenative Coupling (CDC) between Tetrahydroisoquinolines and Activated Methylene Compounds
A novel and efficient C–C bond‐formation method was developed: the cross‐dehydrogenative coupling (CDC) reaction catalyzed by copper bromide in the presence of an oxidizing reagent, tBuOOH. The CDC reaction provides a simple and efficient catalytic method to construct β‐amino diesters and β‐dicyano...
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Veröffentlicht in: | European Journal of Organic Chemistry 2005-08, Vol.2005 (15), p.3173-3176 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A novel and efficient C–C bond‐formation method was developed: the cross‐dehydrogenative coupling (CDC) reaction catalyzed by copper bromide in the presence of an oxidizing reagent, tBuOOH. The CDC reaction provides a simple and efficient catalytic method to construct β‐amino diesters and β‐dicyano amines by a combination of two different sp3 C–H bonds followed by C–C bond formation. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) |
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ISSN: | 1434-193X 1099-0690 |
DOI: | 10.1002/ejoc.200500226 |