A catalytic meta-selective C-H functionalization of 2-phenylpyridines using a range of tertiary halides is described. The protocol is simple to perform and uses commercially available reagents to construct challenging quaternary carbon centres in a regioselective manner. Preliminary studies suggest the C-H functionalization proceeds through a radical process directed via a remote σ-activation.
CITATION STYLE
Paterson, A. J., St John-Campbell, S., Mahon, M. F., Press, N. J., & Frost, C. G. (2015). Catalytic meta-selective C-H functionalization to construct quaternary carbon centres. Chemical Communications, 51(64), 12807–12810. https://doi.org/10.1039/c5cc03951g
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