A New Nickel-Catalyzed Cross-Coupling Reaction between sp3 Carbon Centers
Polyfunctional dialkylzinc compounds and primary alkyl iodides bearing a remote double bond undergo nickel‐catalyzed cross‐coupling even at −35 °C within a few hours, as shown in the example below. The resulting polyfunctional products are formed in good yield. NMP = N‐methyl‐2‐pyrrolidinone, acac =...
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Veröffentlicht in: | Angewandte Chemie International Edition 1996-01, Vol.34 (23-24), p.2723-2725 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng ; jpn |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Polyfunctional dialkylzinc compounds and primary alkyl iodides bearing a remote double bond undergo nickel‐catalyzed cross‐coupling even at −35 °C within a few hours, as shown in the example below. The resulting polyfunctional products are formed in good yield. NMP = N‐methyl‐2‐pyrrolidinone, acac = acetylacetonate, Piv = pivaloyl. |
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ISSN: | 0570-0833 1521-3773 |
DOI: | 10.1002/anie.199527231 |