Direct core functionalisation of naphthalenediimides by iridium catalysed C-H borylation

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Abstract

We report the first boron-substituted naphthalenediimides (NDIs), prepared by iridium catalysed C-H activation. When the NDI substrates bear N-benzyl substituents, the naphthyl NDI core is borylated in preference, suggestive of a directed borylation mechanism. Borylated NDIs are substrates for Suzuki-Miyaura couplings and borylation of an NDI bearing two inequivalent N-substituents has also been demonstrated. © 2014 Partner Organisations.

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Lyall, C. L., Shotton, C. C., Pérez-Salvia, M., Pantoş, G. D., & Lewis, S. E. (2014). Direct core functionalisation of naphthalenediimides by iridium catalysed C-H borylation. Chemical Communications, 50(89), 13837–13840. https://doi.org/10.1039/c4cc06522k

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