4.6 Article

Cross-Dehydrogenative-Coupling of Alkoxybenzenes with Toluenes: Copper(II) Halide Mediated Tandem Halo/Benzylation of Arenes

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 22, 期 50, 页码 18169-18178

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201603783

关键词

C-H activation; cross-dehydrogenative-coupling; diarylmethane; homogeneous catalysis; tandem reactions

资金

  1. University of Manchester
  2. EPSRC
  3. Engineering and Physical Sciences Research Council [1237115, EP/G007519/2] Funding Source: researchfish
  4. EPSRC [EP/G007519/2] Funding Source: UKRI

向作者/读者索取更多资源

A cross-dehydrogenative-coupling of alkoxybenzenes and toluenes with concomitant halogenation is reported. Conditions employed were the use of stoichiometric copper halide salts and dialkylperoxides to afford a range of bromoalkoxydi- and triarylmethanes. Preliminary mechanistic studies suggest that the in situ production of haloarenes (or dihaloarenes) followed by a copper-mediated coupling of a benzylic radical is operational.

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