Electron-Transfer-Induced Intramolecular Heck Carbonylation Reactions Leading to Benzolactones and Benzolactams

Abstract A metal-catalyst-free intramolecular Heck carbonylation reaction of benzyl alcohols and benzyl amines with carbon monoxide under heating at 250 °C affords the corresponding benzolactones and benzolactams in good to excellent yields. A hybrid radical/ionic chain mechanism, involving electron...

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Veröffentlicht in:Synthesis (Stuttgart) 2018-08, Vol.50 (15), p.3015-3021
Hauptverfasser: Fukuyama, Takahide, Bando, Takanobu, Ryu, Ilhyong
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract A metal-catalyst-free intramolecular Heck carbonylation reaction of benzyl alcohols and benzyl amines with carbon monoxide under heating at 250 °C affords the corresponding benzolactones and benzolactams in good to excellent yields. A hybrid radical/ionic chain mechanism, involving electron transfer from radical anions generated by nucleophilic attack of alcohols or amines on intermediate acyl radicals, is proposed.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-0037-1609964