4.7 Article

Palladium-Catalyzed Double-Suzuki-Miyaura Reactions Using Cyclic Dibenziodoniums: Synthesis of o-Tetraaryls

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 81, 期 4, 页码 1317-1323

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.5b02255

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资金

  1. National Nature Science Foundation of China (NSFC) [21472213, 21202186]
  2. Croucher Foundation (Hong Kong) in the form of a CAS-Croucher Foundation Joint Laboratory Grant
  3. Innovation Program of Shanghai Municipal Education Commission [14YZ144]

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Palladium-catalyzed double-Suzuki-Miyaura couplings between cyclic dibenziodoniums and arylboronic acids have been developed. As such, a wide range of otetraaryls were synthesized in good to excellent yields of 22-94%. Furthermore, tetraphenylene was prepared in 21% isolated yield with 2,2'-biphenyldiboronic acid by using this method.

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