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Chan D.G., Winternheimer, D.J. and Merlic, C.A. (2011) Enol Silyl Ethers via Copper(II)-Catalyzed C-O Bond Formation. Organic Letters, 13, 2778-2781.
http://dx.doi.org/10.1021/ol2009297

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.