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<dc:title>β-Functionalization of 4a-aza-8a-boranaphthalene via Iridium-catalyzed C-H Borylation</dc:title>
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<dcterms:abstract>A general method for the functionalization of 4a-aza-8a-boranaphthalene in the position ? to the nitrogen atom has been developed. This method is based on a regioselective iridium-catalyzed C?H activation process for the introduction of a boronate group, which can subsequently be transformed into a variety of aryl or alkynyl groups via cross-coupling reactions. Selective mono- or difunctionalization can be achieved by controlling the reaction conditions during the borylation step. The photophysical properties of the obtained 3- or 3,6-substituted BN-naphthalenes have been evaluated, and some of them have been found to be significantly fluorescent, with fluorescence quantum yields up to 0.85.</dcterms:abstract>
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