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Evans, D.A., Katz, J.L. and West, T.R. (1998) Synthesis of Diaryl Ethers through the Copper-Promoted Arylation of Phenols with Arylboronic Acids: An Expedient Synthesis of Thyroxine. Tetrahe-dron Letters, 39, 2937-2940.
http://dx.doi.org/10.1016/S0040-4039(98)00502-4

has been cited by the following article:

• TITLE: Microwave Application and Anhydrous Cu(OAc)2 Mediated O-Arylation of Aliphatic Amino Alcohols

  AUTHORS: Mohammad Al-Masum, Linda Quinones, Laurance T. Cain

  KEYWORDS: Hydroxylamine, Amino Ether, O-Arylation, O-Styrylation, Microwave

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.2, May 27, 2016

  ABSTRACT: Anhydrous Cu(OAc)2 mediated efficient protocol has been developed in the area of C-O coupling from potassium aryltrifluoroborates and aliphatic amino alcohols such as β-hydroxy, γ-hydroxy, and δ-hydroxy amines. The scope of this transformation focuses on direct O-arylation and O-styrylation. The reaction vial loaded with reactants under argon atmosphere is microwaved at 140°C for 30 min to furnish the corresponding cross-coupling product, amino ethers, in good yields.