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    Reaction of pentafluorobenzoylpyruvic acid with amines [Electronic resource] / V. I. Saloutin, I. T. Bazyl, Z. E. Skryabina, P. N. Kondrat'ev, O. N. Chupakhin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1994. - Vol. 43, № 2. - P279-282
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CYCLIZATION -- INTRAMOLECULAR CYCLIZATION -- PRIMARY AMINES -- PENTAFLUOROBENZOYLPYRUVIC ACID
Аннотация: Reactions of pentafluorobenzoylpyruvic acid with amines afford the respective enamines. The intramolecular cyclization of the latter results in N-substituted 4-quinolone-2-carboxylic acids. Ammonia and triethylamine favor the cyclization of pentafluorobenzoylpyruvic acid to 2-carboxychromone.

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