1994
DOI: 10.1007/bf00695829
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Reaction of pentafluorobenzoylpyruvic acid with amines

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Cited by 5 publications
(3 citation statements)
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“…2-Amino-substituted 3-pentafluorobenzoyl acrylic acids 48 derived from pyruvic acid 47 were found to undergo an intramolecular cyclization into fluoro-4-quinolone-2-carboxylic acids 49 (Scheme 16) [49][50][51].…”
Section: Fluorinated Benzazinesmentioning
confidence: 99%
“…2-Amino-substituted 3-pentafluorobenzoyl acrylic acids 48 derived from pyruvic acid 47 were found to undergo an intramolecular cyclization into fluoro-4-quinolone-2-carboxylic acids 49 (Scheme 16) [49][50][51].…”
Section: Fluorinated Benzazinesmentioning
confidence: 99%
“…2-Amino-substituted 3-pentafluorobenzoyl acrylic acids 48 derived from pyruvic acid 47 were found to undergo an intramolecular cyclization into fluoro-4-quinolone-2-carboxylic acids 49 (Scheme 16) [49][50][51].…”
Section: Scheme 12mentioning
confidence: 99%
“…However, these products are formed following different heterocyclization paths: cyclocondensation of pentafluorobenzoylpyruvate I with hydrazines involves the β-dicarbonyl fragment to give ethyl 5-pentafluorophenylpyrazole-3-carboxylates [4], while 3-methylidene-2,4-dioxobutanoates II and III undergo cyclization with participation of the α-oxovinyl moiety.…”
mentioning
confidence: 99%