Abstract
The SET-induced biaryl cross-coupling reaction is established as the first example of a Grignard SRN1 reaction. The reaction is examined within the mechanistic framework of dissociative electron transfer in the presence of a Lewis acid. DFT calculations show that the reaction proceeds through a radical intermediate in the form of an Mg ion-radical cage, which eludes detection in trapping experiments by reacting quickly to form an MgPh2 radical anion intermediate. A new mechanism is proposed. © 2014 American Chemical Society.
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CITATION STYLE
Haines, B. E., & Wiest, O. (2014). SET-induced biaryl cross-coupling: An SRN1 reaction. Journal of Organic Chemistry, 79(6), 2771–2774. https://doi.org/10.1021/jo500222d
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