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ChemInform 2011, 42, issue 37 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Phenol ethers Q 0270 DOI: 10.1002/chin.201137064 An Efficient Fluoride-Mediated O-Arylation of Sterically Hindered Halophenols with Silylaryl Triflates under Mild Reaction Conditions. — Notable features of the diaryl ether synthesis include no need for transition metal catalysts and tolerance of ha- lide substituents. — (GEBARA, K. S.; CASAGRANDE, G. A.; RAMINELLI*, C.; Tetrahedron Lett. 52 (2011) 22, 2849-2852, http://dx.doi.org/10.1016/j.tetlet.2011.03.124 ; Fac. Cienc. Exatas Tecnol., Univ. Fed. Grande Dourados, Rodovia Dourados, Brazil; Eng.) — Mais 37- 064

ChemInform Abstract: An Efficient Fluoride-Mediated O-Arylation of Sterically Hindered Halophenols with Silylaryl Triflates under Mild Reaction Conditions

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Page 1: ChemInform Abstract: An Efficient Fluoride-Mediated O-Arylation of Sterically Hindered Halophenols with Silylaryl Triflates under Mild Reaction Conditions

Phenol ethersQ 0270 DOI: 10.1002/chin.201137064

An Efficient Fluoride-Mediated O-Arylation of Sterically Hindered Halophenols with Silylaryl Triflates under Mild Reaction Conditions. — Notable features of the diaryl ether synthesis include no need for transition metal catalysts and tolerance of ha-lide substituents. — (GEBARA, K. S.; CASAGRANDE, G. A.; RAMINELLI*, C.; Tetrahedron Lett. 52 (2011) 22, 2849-2852, http://dx.doi.org/10.1016/j.tetlet.2011.03.124 ; Fac. Cienc. Exatas Tecnol., Univ. Fed. Grande Dourados, Rodovia Dourados, Brazil; Eng.) — Mais

37- 064

ChemInform 2011, 42, issue 37 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim