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- W2090421357 abstract "2-Cyano-3-hydroxyquinoxaline 1-oxide (Ia), and its 7-chloro- or 7-ethoxy-derivatives (Ib, c), on treatment with aniline, are deoxygenated, with a simultaneous displacement of the nitrile group, resulting in the formation of 2-anilino-quinoxalines (IIa, e and f). Ia undergoes similar transformations with N-methylaniline and cyclohexylamine. The N-oxide (Ia), on being heated with fuming hydrobromic acid, yields 6-bromo-2,3-dihydroxyquinoxaline (IVa), the mechanism of formation of which has been outlined." @default.
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- W2090421357 date "1965-04-01" @default.
- W2090421357 modified "2023-10-16" @default.
- W2090421357 title "Quinoxaline Derivatives. V. Some Reactions of 2-Cyano-3-hydroxyquinoxaline 1-Oxide" @default.
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- W2090421357 doi "https://doi.org/10.1246/bcsj.38.562" @default.
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