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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CITATION STYLE
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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