PIDA‐Promoted Selective C 5 C−H Selenylations of Indolines via Weak Interactions
An efficient PIDA (phenyliodine(III) diacetate)‐promoted positional selective C−H selenylations of indolines with diaryl diselenides has been developed. This transformation conducted under mild reaction conditions with a broad functional group tolerance, thus providing an efficient protocol to selen...
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Veröffentlicht in: | Advanced synthesis & catalysis 2019-11, Vol.361 (21), p.4998-5004 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | An efficient PIDA (phenyliodine(III) diacetate)‐promoted positional selective C−H selenylations of indolines with diaryl diselenides has been developed. This transformation conducted under mild reaction conditions with a broad functional group tolerance, thus providing an efficient protocol to selenylated indolines. Preliminary mechanistic studies indicated a SET pathway was likely involved in this selenylation reaction.
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ISSN: | 1615-4150 1615-4169 |
DOI: | 10.1002/adsc.201900766 |