An intramolecular arene alkylation
reaction has been developed
using the organic photocatalyst 4CzIPN, visible light, and N-(acyloxy)phthalimides as radical precursors. Reaction
conditions were optimized via high-throughput experimentation, and
electron-rich and electron-deficient arenes and heteroarenes are viable
reaction substrates. This reaction enables access to a diverse set
of fused, partially saturated cores which are of high interest in
synthetic and medicinal chemistry.
Triplet-triplet annihilation photon upconversion (TTA-UC) is a photophysical process in which the energy of two photons are combined into a single photon of higher energy. While this strategy has been recognized in applications ranging from bioimaging to solar energy conversion, its uses in synthetic organic chemistry have not been extensively developed. Here, we present a short tutorial on the theoretical underpinnings and the design principles of TTA-UC systems. Selected applications are then discussed to highlight key features of the TTA mechanism, along with a prospective discussion of the potential of these mechanisms to enable innovation in photocatalysis, methods development, and synthetic organic chemistry.
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