4.7 Article

Copper-Mediated Dehydrogenative Biaryl Coupling of Naphthylarnines and 1,3-Azoles

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 78, 期 21, 页码 11045-11052

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jo402078q

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  1. MEXT
  2. JSPS, Japan
  3. Grants-in-Aid for Scientific Research [24106728, 25620084] Funding Source: KAKEN

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A copper-mediated dehydrogenative biaryl cross-coupling of naphthylamines and 1,3-azoles has been developed. The key to its success is the introduction of N,N-bidentate coordination system based on the picolinamide directing group. The reaction proceeds smoothly without precious transition metal catalysts and provides highly pi-extended heterobiaryls directly.

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