N-Hydroxyphthalimide: a new photoredox catalyst for [4+1] radical cyclization of N-methylanilines with isocyanides
The first utilization of N-hydroxyphthalimide (NHPI) as an organophotoredox catalyst is demonstrated by the [4+1] radical cyclization reaction of N-methylanilines with isocyanides. The protocol offers an operationally simple one-pot synthesis of 3-iminodihydroindoles at room temperature.
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2016-01, Vol.52 (70), p.10621-10624 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The first utilization of N-hydroxyphthalimide (NHPI) as an organophotoredox catalyst is demonstrated by the [4+1] radical cyclization reaction of N-methylanilines with isocyanides. The protocol offers an operationally simple one-pot synthesis of 3-iminodihydroindoles at room temperature. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c6cc04846c |