Iodoarene-catalyzed oxidative transformations using molecular oxygen
Molecular oxygen serves as a useful oxidant for the glycol scission of 1,2-diols and the Hofmann rearrangement of primary amides using pentamethyliodobenzene as a catalyst. The use of isobutyraldehyde and Lewis basic nitriles under O enabled the iodine(i)/(iii) catalytic cycle, where in situ-generat...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2017, Vol.53 (70), p.9781-9784 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Molecular oxygen serves as a useful oxidant for the glycol scission of 1,2-diols and the Hofmann rearrangement of primary amides using pentamethyliodobenzene as a catalyst. The use of isobutyraldehyde and Lewis basic nitriles under O
enabled the iodine(i)/(iii) catalytic cycle, where in situ-generated peracid acts as a terminal oxidant. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c7cc05160c |