Intermolecular 2+2 imine-olefin photocycloadditions enabled by Cu(I)-alkene MLCT

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Abstract

2 + 2 Photocycloadditions are idealized, convergent construction approaches of 4-membered heterocyclic rings, including azetidines. However, methods of direct excitation are limited by the unfavorable photophysical properties of imines and electronically unbiased alkenes. Here, we report copper-catalyzed photocycloadditions of non-conjugated imines and alkenes to produce a variety of substituted azetidines. Design principles allow this base metal-catalyzed method to achieve 2 + 2 imine-olefin photocycloaddition via selective alkene activation through a coordination-MLCT pathway supported by combined experimental and computational mechanistic studies.

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Flores, D. M., Neville, M. L., & Schmidt, V. A. (2022). Intermolecular 2+2 imine-olefin photocycloadditions enabled by Cu(I)-alkene MLCT. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-30393-6

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