4.5 Article

Sterically Encumbered Tetraarylimidazolium Carbene Pd-PEPPSI Complexes: Highly Efficient Direct Arylation of Imidazoles with Aryl Bromides under Aerobic Conditions

Journal

ORGANOMETALLICS
Volume 35, Issue 16, Pages 2655-2663

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.6b00391

Keywords

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Funding

  1. Foundation for Distinguished Young Talents in Higher Education of Guangdong [Yq2013101]
  2. NSFC [21203256, 21473261]
  3. Guangdong Natural Science Funds for Distinguished Young Scholar [2015A030306027]
  4. Project of innovation for enhancing Guangdong Pharmaceutical University
  5. provincial experimental teaching demonstration center of chemistry & chemical engineering
  6. NSFC-Guangdong for Supercomputing Applications

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A series of sterically encumbered tetraarylimidazolium carbene Pd-PEPPSI complexes were conveniently prepared and fully characterized. These sterically encumbered Pd-PEPPSI complexes act as active precatalysts for the direct arylation of imidazoles with aryl bromides under aerobic conditions. The catalytic performance of Pd-PEPPSI complexes in cross-coupling processes is investigated. Under the optimal protocols, the cross-coupling reactions regioselectively produced C5-arylation products in moderate to excellent yields, which could tolerate a wide range of functional aryl bromides.

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