4.7 Article

Highly enantioselective synthesis of silahelicenes using Ir-catalyzed [2+2+2] cycloaddition

期刊

CHEMICAL COMMUNICATIONS
卷 48, 期 9, 页码 1311-1313

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cc16762f

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资金

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan [22350046]
  2. Rohm Foundation
  3. Grants-in-Aid for Scientific Research [22350046] Funding Source: KAKEN

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Silahelicenes, which contain two silole moieties in a helically chiral structure, were synthesized by a chiral Ir-catalyzed intermolecular [2 + 2 + 2] cycloaddition of tetraynes with diynes along with a Ni-mediated intramolecular [2 + 2 + 2] cycloaddition. The photophysical properties of the obtained highly enantiomerically enriched silahelicenes (up to 93% ee) were also measured.

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