4.6 Article

Investigating N-methoxy-N '-aryl ureas in oxidative C-H olefination reactions: an unexpected oxidation behaviour

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ORGANIC & BIOMOLECULAR CHEMISTRY
卷 9, 期 13, 页码 4736-4740

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ob05636k

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  1. Studienstiftung des deutschen Volkes
  2. NRW Graduate School of Chemistry
  3. Alfried Krupp von Bohlen und Halbach Foundation

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Herein, we report a urea derived directing group for mild and highly selective oxidative C-H bond olefination. Subsequent intramolecular Michael addition affords dihydroquinazolinones in good yields. The N-O bond of the urea substrate exhibits superior oxidative behaviour compared to a variety of other external oxidants.

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