Synthesis of highly substituted tetrahydrofurans by catalytic polar-radical-crossover cycloadditions of alkenes and alkenols

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Abstract

Light up my ring: The title reaction is catalyzed by an acridinium/phenylmalononitrile photoredox system. A variety of readily available olefins and unsaturated alcohols can be employed to furnish tetrahydrofuran adducts with complete regiocontrol and up to four contiguous stereogenic centers. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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APA

Grandjean, J. M. M., & Nicewicz, D. A. (2013). Synthesis of highly substituted tetrahydrofurans by catalytic polar-radical-crossover cycloadditions of alkenes and alkenols. Angewandte Chemie - International Edition, 52(14), 3967–3971. https://doi.org/10.1002/anie.201210111

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