Palladium(III)-Catalyzed Fluorination of Arylboronic Acid Derivatives
Anthony R. Mazzotti, Michael G. Campbell, Pingping Tang, Jennifer M. Murphy and Tobias Ritter*
*Department of Chemistry and Chemical Biology, Harvard
University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States, Email:
ritter
chemistry.harvard.edu
A. R. Mazzotti, M. G. Campbell, P. Tang, J. M. Murphy, T. Ritter, J. Am. Chem. Soc., 2013, 135, 14012-14015.
DOI: 10.1021/ja405919z
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Abstract
A palladium-catalyzed synthesis of aryl fluorides from arylboronic acid derivatives is operationally simple and amenable to multigram-scale synthesis. Evaluation of the reaction mechanism suggests a single-electron-transfer pathway that involves a Pd(III) intermediate.
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Key Words
ID: J48-Y2013
