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NMR-Spektroskopie an Heterocyclen, 6. Mitt. Favorskii-Umlagerung von α-Brom-β-methoxy-ketonen bei der Imidazol-Cyclisierung in flüssigem Ammoniak
Authors:Hans-Joachim Sattler  Hans-Gerd Lennartz  Walter Schunack
Abstract:NMR Spectroscopy of Heterocycles. VI: Favorskii Rearrangement of α-Bromo-β-methoxy Ketones During Imidazole Cyclisation in Liquid Ammonia. During imidazole synthesis with α-bromo ketones and formiminic ethyl ester in liquid ammonia α-alkylbutyric amides were obtained as by-products. Their formation is attributed to a Favorskii rearrangement. The compounds were investigated by NMR spectroscopy.
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