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We report an enantioselective approach toward new planar-chiral azaboroles bearing the [2.2]paracyclophane unit and studies of their (chir)optical properties. Fusing the planar-chiral scaffold with a B,N-heterocycle led to the formation of a set of three substances, all of which have interesting chiroptical properties (glum up to 4.7 × 10–3 and BCPL up to 3.1 M–1 cm–1). 1a exhibits superior fluorescence in the solid state unlike the rest of the series.
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Koudelka et al. (2026) studied this question.
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