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- W2090259511 startingPage "2960" @default.
- W2090259511 abstract "N-Phenyl-C-(6-uracilyl)nitrone (II) was prepared in 80% yield from orotaldehyde (I) and phenylhydroxylamine. II underwent 1,3-dipolar cycloaddition reactions with several ethylenic and acetylenic compounds to afford the corresponding isoxazolidines (IIIa—f) and isoxazolines (IVg—i). Similar reactions of II with phenyl isocyanate, carbon disulfide and with enamine were carried out successfully. The structural elucidation of these products was done on the basis of their NMR spectra." @default.
- W2090259511 created "2016-06-24" @default.
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- W2090259511 date "1968-12-01" @default.
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- W2090259511 title "Studies on Heteroaromaticity. XXI. 1,3-Dipolar Cycloaddition of<i>N</i>-Phenyl-<i>C</i>-(6-uracilyl)nitrone" @default.
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- W2090259511 doi "https://doi.org/10.1246/bcsj.41.2960" @default.
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