4.6 Article

Chelation-Assisted Cross-Coupling of Anilines through In Situ Activation as Diazonium Salts with Boronic Acids under Ligand-, Base-, and Salt-Free Conditions

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 19, 期 28, 页码 9291-9296

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201300858

关键词

aniline; boronic acid; cross-coupling; density functional calculations; diazonium salt; palladium

资金

  1. Universite de Nantes
  2. Centre National de la Recherche Scientifique (CNRS)
  3. Agence Nationale de la Recherche [ANR JCJC 7141]
  4. Institut Universitaire de France (IUF)

向作者/读者索取更多资源

We describe the coupling of anilines with aryl boronic acids, under ligand-, base-, and salt-free conditions at room temperature. This new reaction proceeds through the formation of an aryl palladium alkoxo complex, which allows the transmetalation step with aryl boronic acids without any external base. Importantly, this sustainable procedure generates only environmentally friendly byproducts such as tBuOH, H2O, N2, and B(OH)3. The reaction mechanism has been deeply investigated through experimental and theoretical studies.

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