Enantioselective cyanation of propargylic C-H bonds via cooperative photoredox and copper catalysis
Herein, we report an enantioselective cyanation of propargylic C-H bonds by combining photoredox catalysis with a copper-catalyzed radical relay in which the propargylic radical was generated by an intramolecular 1,5-HAT process. This reaction provides easy access to optically pure propargyl nitrile...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2023-04, Vol.59 (31), p.4656-4659 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Herein, we report an enantioselective cyanation of propargylic C-H bonds by combining photoredox catalysis with a copper-catalyzed radical relay in which the propargylic radical was generated by an intramolecular 1,5-HAT process. This reaction provides easy access to optically pure propargyl nitrile compounds under mild conditions. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d3cc00410d |