4.3 Article

Decarboxylative trifluoromethylation of aryl halides using well-defined copper-trifluoroacetate and -chlorodifluoroacetate precursors

Journal

JOURNAL OF FLUORINE CHEMISTRY
Volume 131, Issue 11, Pages 1108-1112

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2010.04.005

Keywords

Trifluoromethylation; Organometallic; Copper

Funding

  1. Office of Basic Energy Sciences of the U S Department of Energy [DE-FG02-07ER15885]

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New synthetic routes to (NHC)copper-trifluoroacetate and -chlorodifluoroacetate complexes were developed (NHC = N-heterocyclic carbenes) so baseline reactivity patterns could be established for the decarboxylative trifluoromethylation of organic halides In the presence of aryl halides loss of CO2 from these new precursors occurred at 160 C concurrent with the formation of aryl-CF3 (C) 2010 Elsevier BV All rights reserved

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