首页> 外文期刊>Collection of Czechoslovak Chemical Communications >REACTION OF PYRYLIUM SALTS WITH NUCLEOPHILES .24. NEW MONO- AND BISPYRIDINIUM SALTS WITH A CENTRAL 2,5-DIARYLOXAZOLE GROUP
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REACTION OF PYRYLIUM SALTS WITH NUCLEOPHILES .24. NEW MONO- AND BISPYRIDINIUM SALTS WITH A CENTRAL 2,5-DIARYLOXAZOLE GROUP

机译:吡咯盐与核的反应.24。具有中心2,5-二芳恶唑基团的新单和双吡啶鎓盐

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摘要

Reduction of nitro substituted 2,5-diaryloxazoles with hydrazine hydrate and Raney nickel affords in good yield 2,5-diaryloxazoles having amino group(s) on the aryl ring(s). The reaction of 2,4,6-tri-substituted pyrylium perchlorates with mono-and diamino-2,5-diaryloxazoles yields new mono- and bispyridinium perchlorates with a central 2,5-diaryloxazole group. Their electronic, C-13 NMR and H-1 NMR spectra are presented and discussed. [References: 30]
机译:用水合肼和阮内镍还原硝基取代的2,5-二芳基恶唑可得到良好收率的芳基环上具有氨基的2,5-二芳基恶唑。 2,4,6-三取代高氯酸吡啶鎓与单和二氨基-2,5-二芳基恶唑的反应产生了新的具有中央2,5-二芳基恶唑基团的新的单和双吡啶鎓高氯酸盐。介绍并讨论了它们的电子图,C-13 NMR和H-1 NMR光谱。 [参考:30]

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