Synthesis of α‑Aryl Primary Amides from α‑Silyl Nitriles and Aryl Sulfoxides through [3,3]-Sigmatropic Rearrangement
A simple and efficient protocol was developed for the preparation of challenging α-aryl primary amides. This metal-free coupling process was triggered by TfOH-promoted electrophilic activation of α-silyl nitrile to generate keteniminium ion species, followed by reaction with aryl sulfoxide through [...
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Veröffentlicht in: | Organic letters 2022-03, Vol.24 (8), p.1700-1705 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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