4.6 Article

NCP pincer palladacycle as a phosphine-free catalyst precursor for the Heck-Mizoroki coupling of aryl halides

Journal

RSC ADVANCES
Volume 2, Issue 12, Pages 5080-5083

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ra01261h

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Funding

  1. CNPq
  2. FAPERGS
  3. CAPES (Brazil)

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NCP pincer palladacycle 1 has been reported as an excellent catalyst precursor for the Suzuki-Miyaura reaction. Now, it's properties have been evaluated in the Heck reaction. 1 is highly active for the coupling of ArI, ArBr and electron-poor ArCl with n-butyl acrylate showing limitations in the reaction of deactivated ArCl and sterically hindered olefins.

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