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- W2016814446 abstract "Pyridyl-3-arylaminoisoxazol-5(2H)-ones, substituted on N with a nitropyridine group 12a-12e reacted with triethylamine in ethanol under reflux to give imidazo(1,2-a)pyridines 13a-13e and carbon dioxide. An analogous synthesis failed to yield ethyl 3-(2-ethoxycarbonylphenyl) amino- 5-oxo-2,5-dihydroisoxazole-4-carboxylate; the reaction of diethyl (2- ethoxycarbonylphenyl)thiocarbamoylmalonate with hydroxylamine gave the novel isoxazolo(3,2-b)quinazoline 14 by intramolecular acylation of the isoxazolone intermediate 14a." @default.
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- W2016814446 date "2005-06-13" @default.
- W2016814446 modified "2023-09-27" @default.
- W2016814446 title "Synthesis of imidazo[1,2-a] pyridines by rearrangement of 2-pyridyl-3-arylaminoisoxazol-5-(2H)-ones" @default.
- W2016814446 cites W1522110495 @default.
- W2016814446 doi "https://doi.org/10.3998/ark.5550190.0006.e07" @default.
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