Preparation of beta-and gamma-lactams via ring closures of unsaturated carbamoyl radicals derived from 1-carbamoyl-1-methylcyclohexa-2,5-dienes

1-Carbamoyl-1-methylcyclohexa-2,5-dienes produced the corresponding delocalised 1-carbamoyl-1-methylcyclohexa-2,5-dienyl radicals on treatment with radical initiators. At temperatures above ca. 300 K dissociation to produce toluene and aminoacyl (carbamoyl) radicals took place. The alternative disso...

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Veröffentlicht in:	Organic & biomolecular chemistry 2004-02, Vol.2 (3), p.421-428
Hauptverfasser:	Franco Bella, A, Jackson, Leon V, Walton, John C
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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