4.6 Article

Enantioselective Synthesis of Fully Benzenoid Single and Double Carbohelicenes via Gold-Catalyzed Intramolecular Hydroarylation

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 24, Issue 21, Pages 5434-5438

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201800986

Keywords

asymmetric catalysis; carbohelicenes; circularly polarized luminescence; gold; hydroarylation

Funding

  1. ACT-C from JST, Japan [JPMJCR1122YR]
  2. JSPS, Japan [JP26102004]
  3. Grants-in-Aid for Scientific Research [26102004] Funding Source: KAKEN

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The enantioselective synthesis of fully benzenoid single and double carbo[6]helicenes has been achieved via the gold-catalyzed intramolecular hydroarylation. The single crystal of the racemic double carbo[6]helicene consists of unique layer structures like timbers with halving joints in the woodworking. Furthermore, the double carbo[6]helicenes exhibited relatively large CPL activities among chiral small organic molecules.

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