Demonstrates tunable fluorescence in indole-fused isocoumarin, suggesting new synthetic routes.
Employing indole as a synthon in tandem annulation for the construction of polycyclic skeletons remains challenging because of its oxidative dimerization. Herein, we report an ultrafast (5 min) Ir/Cu-catalyzed tandem oxidative [4 + 2] annulation of aromatic acids with indoles, delivering planar indole-fused isochromenes with tunable fluorescence. This transformation involves sequential intermolecular CDC with exclusive C3 selectivity of indoles and intramolecular CDC. Notably, the products can be readily converted to 3-spirooxindole, featuring solvent- and concentration-dependent fluorescence emission properties.
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Li et al. (2026) studied this question.
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