Acid promoted radical-chain difunctionalization of styrenes with stabilized radicals and (N,O)-nucleophiles.

Chem Commun (Camb)

Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, Germany.

Published: February 2020

A difunctionalization of alkenes through sequential addition of a radical and a nucleophile has been developed, which is suggested to proceed by a radical chain mechanism not requiring a catalyst. An electron transfer step to the oxidant benzoyl peroxide is facilitated by protonation with a strong acid.

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http://dx.doi.org/10.1039/c9cc09369aDOI Listing

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