Flow photochemical Giese reaction via silane-mediated activation of alkyl bromides

Fanini, F;Luridiana, A;Mazzarella, D;Alfano, AI;van der Heide, P;Rincon, JA;Garcia-Losada, P;Mateos, C;Frederick, MO;Nuno, M;Noel, T

2023-01-01

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Abstract

Organic halides play a key role as building blocks in synthesis because of their low cost and wide avail-ability. In recent years, halogen-atom transfer (XAT) has emerged as a reliable approach to exploit these substrates in radical processes. Herein, we report a hydroalkylation of electron-poor olefins using alkyl bromides based on a UVA-induced silane-mediated XAT reaction. Our protocol is operationally simple, displays a broad scope and does not require a photocatalyst. Flow technology was used to reduce the reaction times and scale the process. Notably, a two-step protocol, combining the XAT protocol with a subsequent Horner-Wadsworth-Emmons reaction, has been developed to enable the allylation of C (sp3)-Br bonds.