4.8 Article

Triarylphosphines as Aryl Donors for Pd(II)-Catalyzed Aromatic Coupling of Oxabenzonorbornadienes

Journal

ORGANIC LETTERS
Volume 17, Issue 18, Pages 4628-4631

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b02366

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Funding

  1. Hundred Talent Program of Chinese Academy of Sciences (CAS)
  2. Natural Science Foundation of Jiangsu [BK20151235]

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A new approach was developed for Pd(II)-catalyzed aromatic coupling of oxabenzonorbornadienes with triarylphosphines as both ligands and aryl donors. Diverse functional groups including halo- (F-, Cl-, and Br-), CF3-, and furyl groups are well tolerated. For unsymmetrical triarylphosphines, the migration ability of aryls is consistent with the electronic property of substituents and maintains the order EDG-Ar > H-Ar > EWD-Ar (EDG means electron-donating group, EWG means electron-withdrawing group). A preliminary mechanistic study was also disclosed.

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