Flow Giese reaction using cyanoborohydride as a radical mediator

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Abstract

Tin-free Giese reactions, employing primary, secondary, and tertiary alkyl iodides as radical precursors, ethyl acrylate as a radical trap, and sodium cyanoborohydride as a radical mediator, were examined in a continuous flow system. With the use of an automated flow microreactor, flow reaction conditions for the Giese reaction were quickly optimized, and it was found that a reaction temperature of 70 °C in combination with a residence time of 10-15 minutes gave good yields of the desired addition products. © 2013 Fukuyama et al.

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Fukuyama, T., Kawamoto, T., Kobayashi, M., & Ryu, I. (2013). Flow Giese reaction using cyanoborohydride as a radical mediator. Beilstein Journal of Organic Chemistry, 9, 1791–1796. https://doi.org/10.3762/bjoc.9.208

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