Palladium-Catalyzed C–H Activation Taken to the Limit. Flattening an Aromatic Bowl by Total Arylation

  • Qianyan Zhang
    Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467-3860, United States
  • Katsuaki Kawasumi
    Department of Chemistry, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
  • Yasutomo Segawa
    Department of Chemistry, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
  • Kenichiro Itami
    Department of Chemistry, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan
  • Lawrence T. Scott
    Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467-3860, United States

書誌事項

公開日
2012-09-14
DOI
  • 10.1021/ja306992k
公開者
American Chemical Society (ACS)

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説明

All 10 C-H positions on the rim of corannulene can be arylated by repetitive palladium-catalyzed C-H activation. To relieve congestion among the 10 tightly packed aryl substituents in the product, the central corannulene adopts a nearly planar geometry.

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